Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94276

21 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 20, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Zimmer, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

21 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-04

Z-1709-2024
Recall number
Z-1709-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088498(17)321205(10)65620069 (01)00889024088498(17)321205(10)65635922 (01)00889024088498(17)321205(10)65635923 (01)00889024088498(17)330111(10)65674071 (01)00889024088498(17)330115(10)65674072 (01)00889024088498(17)330428(10)66010704 (01)00889024088498(17)330730(10)66166096 (01)00889024088498(17)330822(10)66216633 Lot Numbers: 65620069 65635922 65635923 65674071 65674072 66010704 66166096 66216633

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 2 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-06

Z-1710-2024
Recall number
Z-1710-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088504(17)330115(10)65703586 (01)00889024088504(17)330307(10)65703587 (01)00889024088504(17)331124(10)66247618 (01)00889024088504(17)331124(10)66247619 Lot Numbers: 65703586 65703587 66247618 66247619

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 3 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-08

Z-1711-2024
Recall number
Z-1711-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088511(17)300725(10)64811254 (01)00889024088511(17)300803(10)64811255 (01)00889024088511(17)330211(10)65834885 Lot Numbers: 64811254 64811255 65834885

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 4 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-10

Z-1712-2024
Recall number
Z-1712-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088528(17)330527(10)66060712 Lot Numbers: 66060712

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 5 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-12

Z-1713-2024
Recall number
Z-1713-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088535(17)290809(10)64475610 (01)00889024088535(17)310331(10)65038408 (01)00889024088535(17)310324(10)65038409 (01)00889024088535(17)310915(10)65209412 (01)00889024088535(17)310915(10)65209413 Lot Numbers: 64475610 65038408 65038409 65209412 65209413

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 6 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 16 Holes, 236 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-16

Z-1714-2024
Recall number
Z-1714-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088559(17)290804(10)64475611 (01)00889024088559(17)290806(10)64475612 Lot Numbers: 64475611 64475612

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 7 of 21

ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 7-2357-018-04

Z-1715-2024
Recall number
Z-1715-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088566(17)290409(10)64325922 (01)00889024088566(17)290414(10)64325923 (01)00889024088566(17)290515(10)64396817 (01)00889024088566(17)290517(10)64396818 (01)00889024088566(17)290831(10)64464677 (01)00889024088566(17)300325(10)64714915 (01)00889024088566(17)300330(10)64714916 (01)00889024088566(17)300321(10)64714917 (01)00889024088566(17)320329(10)65324701 (01)00889024088566(17)320510(10)65387353 (01)00889024088566(17)330220(10)65716463 (01)00889024088566(17)330127(10)65716464 (01)00889024088566(17)330426(10)65982902 (01)00889024088566(17)330426(10)66010705 Lot Numbers: 64325922 64325923 64396817 64396818 64464677 64714915 64714916 64714917 65324701 65387353 65716463 65716464 65982902 66010705

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 8 of 21

ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-06

Z-1716-2024
Recall number
Z-1716-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088573(17)290510(10)64370380 (01)00889024088573(17)290517(10)64370382 (01)00889024088573(17)290607(10)64423329 (01)00889024088573(17)290811(10)64475643 (01)00889024088573(17)300225(10)64661551 (01)00889024088573(17)300307(10)64661552 (01)00889024088573(17)300511(10)64745739 (01)00889024088573(17)300506(10)64745742 (01)00889024088573(17)300506(10)64745744 (01)00889024088573(17)300506(10)64745745 (01)00889024088573(17)321209(10)65635924 (01)00889024088573(17)321207(10)65645147 (01)00889024088573(17)330215(10)65755766 (01)00889024088573(17)330430(10)65997131 (01)00889024088573(17)330428(10)65997134 (01)00889024088573(17)330430(10)66023658 (01)00889024088573(17)330730(10)66166098 (01)00889024088573(17)330811(10)66201200 (01)00889024088573(17)330822(10)66233083 (01)00889024088573(17)330822(10)66233084 Lot Numbers: 64370380 64370382 64423329 64475643 64661551 64661552 64745739 64745742 64745744 64745745 65635924 65645147 65755766 65997131 65997134 66023658 66166098 66201200 66233083 66233084

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 9 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-08

Z-1717-2024
Recall number
Z-1717-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088580(17)300112(10)64568169 (01)00889024088580(17)300307(10)64697763 (01)00889024088580(17)300225(10)64697764 (01)00889024088580(17)330215(10)65755769 (01)00889024088580(17)330218(10)65782566 (01)00889024088580(17)330211(10)65782567 (01)00889024088580(17)331208(10)66233085 Lot Numbers: 64568169 64697763 64697764 65755769 65782566 65782567 66233085

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 10 of 21

ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-10

Z-1718-2024
Recall number
Z-1718-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088597(17)321205(10)65588868 (01)00889024088597(17)330414(10)65943457 (01)00889024088597(17)330512(10)66034781 Lot Numbers: 65588868 65943457 66034781

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 11 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 12 Holes, 184 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-12

Z-1719-2024
Recall number
Z-1719-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088603(17)290512(10)64381071 (01)00889024088603(17)310324(10)65038410 (01)00889024088603(17)310324(10)65038411 (01)00889024088603(17)310324(10)65038412 (01)00889024088603(17)310821(10)65193244 (01)00889024088603(17)311018(10)65233124 (01)00889024088603(17)311017(10)65233125 Lot Numbers: 64381071 65038410 65038411 65038412 65193244 65233124 65233125

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 12 of 21

ZPLP Distal Lateral Fibular Plate, Left, 14 Holes, 210 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-14

Z-1720-2024
Recall number
Z-1720-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088610(17)290730(10)64381072 (01)00889024088610(17)300208(10)64661553 Lot Numbers: 64381072 64661553

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 13 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 16 Holes, 236 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-16

Z-1721-2024
Recall number
Z-1721-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI: (01)00889024088627(17)290930(10)64464711 (01)00889024088627(17)330502(10)66010706 Lot Numbers: 64464711 66010706

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 14 of 21

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-017-04

Z-1722-2024
Recall number
Z-1722-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

GTIN: 00889024055865 Lot Numbers: 64370265 64370266 64370267 64370268 64370269 64370270 64370271 64370279 64370280 64370281 64370289 64370290 64370291 64370292 64370293 64370299 64370301 64370303 64370305 64370307 64475227 64475228 64475252 64475276 64475298 64475306 64475320 64475324 64475359 64475360 64475379 64475383 64528443 64528464 64528481 64528482 64528483 64528484 64528485 64528486 64528487 64528488 64528489 64528490 64528491 64528492 64528493 64528494 64528495 64552845 64552846 64552847 64552848 64552892 64552893 64552895 64552896 64552897 64552898 64552899 64552907 64552909 64552912 64552914 64552921 64553013 64553015 64553020 64553022 64553024 64553029 64553032 64553034 64553037 64563320 64563321 64563324 64563325 64563327 64572555 64572556 64572557 64572558 64572559 64572560 64572561 64572562 64572564 64572565 64572566 64572567 64572568 64572569 64572570 64572571 64572572 64572573 64572574 64572576 64572577 64572578 64572579 64572580 64572581 64572582 64572584 64588261 64588262 64588263 64588264 64588265 64588266 64588267 64751424 64751425 64751427 64751429 64751430 64751431 64751432 64751433 64751435 64751437 64751438 64751439 64751441 64751443 64751444 64751446 64751448 64751450 64751451 64751452 64782498 64782499 64789160 64789161 64789162 64789163 64789164 64789165 65074888 65074889 65074890 65074891 65074892 65074893 65074894 65074895 65074896 65074897 65074898 65074899 65074901 65074902 65074903 65172472 65172473 65172474 65172475 65172476 65172477 65172480 65172481 65172482 65172483 65172484 65172485 65206077 65206078 65206079 65206080 65206081 65206082 65206083 65206084 65206085 65206086 65206087 65206088 65214162 65214163 65214164 65214165 65214166 65214167 65214168 65214170 65214171 65214172 65214174 65214175 65214177 65214180 65214185 65214187 65214189 65214190 65214191 65214192 65214193 65214194 65214196 65214209 65240918 65240919 65240920 65240921 65240922 65240923 65240924 65240925 65240933 65240934 65240935 65240936 65240937 65240938 65240939 65240940 65240941 65240942 65240943 65240944 65240945 65240946 65240947 65240948 65240949 65240950 65240951 65240952 65240957 65240958 65240959 65240960 65240961 65240962 65240963 65240964 65240965 65240966 65240967 65240968 65240969 65240970 65240971 65240972 65240973 65240974 65240975 65240976 65240977 65240978 65240979 65240980 65240981 65240982 65240983 65240984 65240985 65240986 65240987 65240988 65305024 65305025 65305026 65305027 65305028 65305029 65305030 65305031 65305032 65305033 65305034 65305035 65305036 65322055 65322057 65322061 65328490 65328493 65328497 65328500 65335093 65335096 65335099 65335102 65383637 65383640 65383643 65383646 65383649 65383652 65383655 65383659 65383661 65383664 65584568 65584571 65870704 65870705 65934074 65934075 65934076 65934077 65934079 66068464 66068469 66081125 66094419 66094423 66094426 66108599 66121831 66121837 66134362 66134365 66159984 66159988 66159992 66174596 66174599 66187650 66187655 66209322 66209327 66225440 66225443 66225446 66225449 66240671 66240676

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 15 of 21

ZPLP Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-017-06

Z-1723-2024
Recall number
Z-1723-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

GTIN: 00889024055872 Lot Numbers: Lot Number 63579608 63579611 63579634 64403617 64403618 64403619 64403624 64403625 64403626 64403627 64403628 64403629 64403630 64403631 64403632 64403633 64403634 64423729 64423730 64423731 64423732 64423733 64423734 64423735 64423736 64423737 64423738 64423739 64423740 64423741 64423742 64475394 64475399 64528496 64528497 64528498 64528499 64528501 64528502 64528503 64528504 64528505 64528506 64544896 64544898 64544899 64544901 64544902 64544903 64544904 64544905 64544907 64544908 64544909 64544912 64544913 64544915 64544916 64544917 64544919 64544920 64544921 64544922 64544923 64544924 64544925 64544926 64544928 64544929 64572585 64572586 64572587 64572588 64572589 64572590 64572591 64588269 64588270 64588271 64588272 64588273 64588274 64588275 64588276 64588277 64588278 64588279 64588280 64588281 64610599 64610602 64610604 64610605 64610606 64610607 64610608 64610609 64610610 64610611 64610612 64648204 64648205 64648206 64648207 64648208 64648209 64648210 64661052 64732233 64732234 64732235 64732236 64745725 64745726 64745728 64817283 64826538 64826539 64826540 65145488 65145489 65145490 65145492 65145494 65145495 65145497 65145498 65145499 65145502 65145586 65145709 65145764 65145766 65145797 65155431 65155432 65155435 65155436 65155437 65155438 65155439 65155440 65155441 65155442 65155918 65155919 65155920 65155921 65192587 65192588 65192589 65192590 65206091 65206092 65206093 65206094 65206095 65206096 65206097 65206098 65206099 65206101 65206102 65206103 65934061 65934062 65934063 65934064 65934065 65990247 65990252 65990256 65990260 66068473 66081129 66094429 66094432 66094435 66121840 66121844 66121847 66134368 66134371 66174603 66174606 66174608 66187660 66187665 66187670 66194637 66209331 66209336 66240682 66240686 66240689

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 16 of 21

ZPLP Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-017-08

Z-1724-2024
Recall number
Z-1724-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

GTIN: 00889024055889 Lot Numbers: 64475412 64475418 64475422 64475426 64475427 64475428 64475431 64475435 64475439 64475443 64475444 64475445 64475446 64475447 64475448 64475449 64475450 64482031 64482032 64482033 64482034 64482035 64482042 64482043 64482044 64482045 64482046 64482047 64482048 64482051 64482052 64482057 64528508 64528509 64629014 64629015 64629017 64629018 64629019 64629020 64629022 64629023 64629024 64629025 64660057 64660060 64660063 64660066 64660067 64800086 64800087 64800088 64800089 64800090 64800091 64811207 64811208 64811209 64811210 64811212 64811213 64811214 64811215 65060838 65060839 65060840 65060841 65060842 65060843 65060844 65060845 65060846 65060847 65060848 65060849 65060850 65060851 65060852 65060853 65060854 65060855 65074872 65074873 65074874 65074875 65074876 65074877 65192591 65192592 65192593 65192594 65192595 65192596 65192597 65192598 65192599 65192601 65192602 65192603 65229326 65229327 65229328 65229332 65229337 65229341 65229344 65229348 65328548 65537763 65537767 65537771 66108602 66108605 66240694

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 17 of 21

ZPLP Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-017-10

Z-1725-2024
Recall number
Z-1725-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

GTIN: 00889024055896 Lot Numbers: Lot Number 64528516 64528517 64528518 64528522 64528523 64528527 64528528 64528529 64528530 64629028 64629030 64629031 64677270 64677272 64677276 64677278 64677279 64677281 64817167 64817168 64817169 64817170 64817171 64817172 64817173 64817174 64817175 64817176 65021088 65021089 65021090 65021091 65021092 65021093 65092268 65092269 65092270 65092271 65092272 65092273 65092274 65092275 65092276 65092277 65092278 65092279 65192604 65192605 65192606 65192607 65192608 65192609 66174613 66187674 66194640 66194643 66194646 66194649 66194652 66209353 66209363 66240704

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 18 of 21

ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-04

Z-1726-2024
Recall number
Z-1726-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

UDI Number: 00889024055902 Lot Numbers: Lot Number 64362992 64362993 64362994 64362995 64362996 64362997 64362998 64362999 64363001 64363002 64363003 64363004 64363005 64363006 64363007 64363008 64363015 64363016 64363017 64363018 64452231 64452232 64452233 64452234 64452235 64452236 64452237 64452238 64452239 64452240 64452241 64452242 64452243 64452244 64452245 64452246 64452247 64452248 64464613 64464614 64464616 64464618 64464620 64464623 64464625 64464626 64464628 64475451 64475452 64475453 64475454 64475455 64475456 64482183 64482197 64482283 64482341 64482380 64482393 64482402 64482404 64482442 64482484 64537925 64537926 64537927 64537928 64537929 64537936 64537937 64537938 64537939 64537940 64537941 64537942 64537943 64537944 64537945 64537946 64537947 64537948 64537949 64537950 64537951 64537952 64537953 64537954 64537955 64537956 64537957 64537958 64552295 64552296 64552297 64556990 64556991 64557407 64557408 64557411 64557412 64557413 64557414 64563337 64563339 64563341 64563342 64563497 64563523 64563531 64563544 64563546 64563548 64563553 64563554 64563555 64563556 64629033 64629034 64629035 64629036 64629037 64629428 64629429 64629432 64629438 64629440 64629441 64629442 64638181 64638183 64638184 64638185 64638187 64638188 64638189 64638193 64638195 64638373 64638374 64638375 64638377 64638379 64638383 64638440 64638441 64638442 64638443 64638444 64638445 64638446 64638447 64638448 64638449 64638450 64638455 64648164 64648165 64648166 64648167 64648168 64648169 64648173 64648174 64648176 64648177 64648178 64648179 64648180 64648181 64648182 64648186 64648187 64648190 64648191 64648194 64648196 64698164 64698172 64698179 64698183 64698191 64700574 64700575 64700576 64700611 64700612 64732237 64732238 64732239 64732240 64732241 64732251 64732252 64732253 64732254 64732255 64732256 64732257 64732258 64732259 64732260 64739431 64739432 64739433 64739591 64739592 64923371 64923372 64923374 64923376 64923378 64923379 64923381 64923383 64923386 64923388 64923390 64923391 64923392 64923393 64923394 64923395 64923396 64923397 64923398 64923399 64938735 64938737 64938738 64938739 65081467 65081468 65081469 65081470 65081471 65081474 65081489 65081491 65081513 65081515 65081517 65081518 65081521 65081546 65081547 65081548 65081549 65092308 65092309 65092310 65092311 65202505 65202506 65202507 65202508 65202509 65202510 65202511 65202512 65202513 65202514 65202515 65202516 65202518 65225297 65225298 65225299 65225301 65225302 65225303 65225304 65225305 65225306 65225307 65225308 65225309 65225310 65225311 65229428 65229429 65229430 65229431 65241095 65241096 65241097 65241098 65241130 65241131 65241132 65241133 65241134 65241135 65241136 65241137 65305058 65305059 65305060 65305061 65305062 65305063 65305064 65305065 65305066 65305067 65305068 65305069 65322076 65322078 65328551 65328554 65328557 65328559 65328562 65328565 65383708 65383711 65383713 65383719 65383722 65383725 65383727 65383730 65383733 65395909 65395912 65395915 65395918 65395921 65395923 65395926 65395928 65395931 65395934 65395936 65473361 65473364 65507103 65507106 65514361 65521081 65934066 65934067 65934068 65934069 65934070 65934071 65990265 65990269 65990273 66054013 66054018 66054022 66054026 66068476 66094438 66108609

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 19 of 21

ZPLP Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-06

Z-1727-2024
Recall number
Z-1727-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

GTIN: 00889024055919 Lot Numbers: 64403506 64403507 64403508 64403509 64403510 64403511 64403512 64403513 64403514 64403515 64403516 64403517 64403518 64403519 64403520 64403521 64403522 64403523 64403524 64403525 64403526 64423743 64423744 64423745 64496313 64496314 64496315 64496316 64496317 64496318 64496319 64496320 64497330 64497331 64497332 64497333 64497334 64497335 64497336 64497337 64497338 64497411 64497412 64497413 64497414 64497423 64497436 64497439 64497446 64497448 64497449 64497450 64497454 64497455 64497458 64497460 64497461 64497462 64538004 64538005 64538006 64538007 64538008 64538009 64538010 64538011 64538012 64538013 64538014 64538015 64538016 64563586 64563589 64563590 64563592 64563611 64563617 64580493 64580494 64580495 64580496 64580498 64580501 64580503 64581249 64581250 64581251 64581252 64581253 64581254 64581255 64599906 64599907 64599908 64599909 64599910 64599911 64599912 64599913 64599914 64599915 64599916 64599917 64599918 64599925 64599926 64599927 64599957 64599958 64599959 64599960 64599961 64599962 64599963 64629444 64629445 64629446 64629447 64629449 64629450 64629468 64629469 64629470 64629473 64629475 64629476 64629477 64629484 64629485 64629486 64629488 64629489 64629490 64629491 64660068 64660069 64660070 64676547 64676549 64676552 64676555 64676564 64676592 64676593 64676596 64676597 64676599 64676601 64676602 64677064 64677065 64700626 64700639 64700640 64700641 64700649 64700666 64700668 64700670 64700673 64700675 64700678 64700679 64700681 64732261 64732262 64732263 64732264 64732265 64739593 64739594 64739595 64739605 64739606 64739607 64739608 64739609 64739610 64739611 64739612 64739613 64739614 64826552 64826555 64826556 64826557 64826558 64826559 64826560 64844778 64844779 64844780 64844781 64863953 64863955 64863957 64863960 64863962 64863964 64863966 64863968 64863969 64863972 64863978 64863980 64896861 64896866 64896882 64896883 64896884 64896885 64910581 64910583 64910586 64910588 64917619 64917620 64917621 64917622 64917623 64917624 64917625 64917626 64917627 64917628 64938708 64938710 64938711 64938713 64938715 64938716 64938719 64938722 64938741 64938743 64938744 64938746 64973605 64973606 64973607 64973610 64973613 64973615 64973618 64973622 64993145 64993146 64993147 64993148 64993149 64993150 64993151 64993152 64993153 64993165 64993166 64993167 65069753 65069754 65069755 65069756 65069757 65069758 65069759 65069850 65069851 65069852 65081442 65081443 65081444 65081445 65081446 65081447 65081457 65081458 65081459 65081460 65081461 65081462 65092280 65092281 65092282 65092283 65092284 65092285 65092286 65092287 65092288 65092289 65092290 65092291 65092292 65092293 65092294 65092295 65092296 65092297 65092298 65092299 65092301 65092302 65092303 65092304 65092305 65092306 65092307 65192610 65192611 65192612 65192613 65192615 65192616 65192617 65192618 65192619 65192620 65192621 65192622 65192623 65192624 65192625 65192626 65192627 65192628 65192629 65192630 65229432 65229433 65229434 65229435 65241139 65241141 65241142 65241172 65241173 65241174 65241175 65241176 65241177 65241178 65241179 65241180 65305070 65305071 65305072 65305073 65305074 65305075 65305076 65305077 65305078 65305079 65305080 65305081 65322082 65322084 65322086 65322088 65328574 65328578 65328581 65328583 65328587 65328590 65335116 65335119 65335122 65340982 65340985 65340988 65340991 65340994 65383740 65383742 65383745 65383748 65383751 65383753 65383755 65383758 65383761 65383764 65383767 65383770 65395942 65395944 65395946 65507160 65537802 65537808 65537812 65537816 65537818 65537821 65537825 65550439 65934057 65934058 65934059 65934060 66183916

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 20 of 21

ZPLP Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Nonsterile-Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-08

Z-1728-2024
Recall number
Z-1728-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

GTIN: 00889024055926 Lot Numbers: Lot Number 64370324 64370328 64370332 64370333 64370337 64370339 64370341 64370344 64370353 64370354 64370364 64370365 64370366 64370368 64370369 64370370 64406604 64406606 64406609 64406611 64406618 64406619 64406620 64406622 64406625 64406626 64452251 64452252 64452253 64464635 64464647 64464648 64464649 64464651 64464652 64464654 64464656 64464658 64464659 64464660 64464661 64464662 64464664 64464666 64464667 64475555 64475556 64488018 64488021 64488023 64488025 64488028 64488030 64488031 64488032 64488033 64488034 64488035 64488036 64488037 64488038 64538017 64544890 64544891 64544892 64544893 64544894 64544895 64609930 64609931 64609932 64629492 64629494 64629495 64629496 64629518 64629519 64629520 64629522 64629523 64629524 64629525 64629526 64629527 64714907 64714908 64714909 64714912 64714913 64714914 64800035 64800036 64800038 64800041 64800043 64800045 64800047 64800052 64800053 64800054 64800055 64800056 64800057 64800058 64800059 64800060 64800061 64800062 64800077 64800078 64800079 64800080 64800081 64800082 64896819 64896820 64896821 64896823 64896824 64896825 64896826 64896828 64896829 64896846 64896848 64896852 64896853 64896855 64896856 64896858 64896860 64910349 64910350 64910356 64910358 64917592 64917593 64917594 64917595 64917596 64917597 64917598 64917599 64917601 64917602 64917603 64917604 64938529 64938530 64938531 64938532 64938533 64938559 64938595 65021060 65021061 65021062 65021063 65021064 65021065 65021066 65021067 65021068 65021069 65069860 65069861 65069887 65069901 65069902 65241206 65241207 65241208 65305082 65305083 65305084 65305085 65305086 65305087 65305088 65322090 65322092 65328600 65328603 65383773 65383775 65383778 65383779 65383782 65499002 65499005 65521087 65934072 65934073 65977491 65990276

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.

device · product 21 of 21

ZPLP Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Nonsterile-Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-10

Z-1729-2024
Recall number
Z-1729-2024
Initiated
March 20, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Zimmer, Inc.
Quantity
Unavailable

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock, may result in delay in surgery or loss of fixation resulting further intervention

Code information

GTIN: 00889024055933 Lot Numbers: Lot Number 64299456 64299458 64299460 64299461 64299463 64299529 64299530 64299544 64299545 64406629 64406630 64406632 64406633 64406641 64452257 64452258 64452259 64452260 64452261 64452262 64452263 64568257 64568258 64568259 64689556 64689558 64689560 64689562 64689566 64689568 64689570 64689575 64689576 64689577 64689582 64689583 64689584 64689585 64689586 64689587 64697703 64697704 64763352 64763353 64763354 64763355 64763356 64763357 64763358 64763359 64763360 64763361 64763362 64763363 64763364 64763365 64777233 64777234 64777235 64777236 64973578 64973579 64973580 64973581 64973582 64973583 65021094 65021095 65021096 65021097 65021098 65021099 65021102 65021103 65021104 65021105 65021106 65021107 65225324 65232879 65232880 65232881 65232883 65232885 65232889 65305089 65305090 65305091 65305092 65379075 65379077 65379080 65379083 66187074 66187075 66187076 66187077 66187079 66187080 66187081

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, China, Hong Kong, India, Japan, New Zealand, Seoul Korea, Singapore, Switzerland, Taiwan.