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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66499

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

Open FDA event record

Event summary

Timeline bucket
November 05, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
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

8 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 8

FEM COND BUTTRESS PLT, RT.

Z-0585-2014
Recall number
Z-0585-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item #'s: 00-2347-001-12 00-2347-001-14 00-2347-001-16 00-2347-001-18 Lot #s: All lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.

device · product 2 of 8

TIBIO FEM/FEM NAIL.

Z-0586-2014
Recall number
Z-0586-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item Numbers 32-8553-311-11 32-8553-311-13 32-8553-311-15 32-8553-311-17 All lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.

device · product 3 of 8

DIST LAT FEM LOCK PLT, LT

Z-0587-2014
Recall number
Z-0587-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item Number: 47-2357-102-14 47-2357-102-18 All lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.

device · product 4 of 8

DIST LAT FEM LOCK PLT, RT

Z-0588-2014
Recall number
Z-0588-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item Numbers: 47-2357-101-14 47-2357-101-18 47-2357-102-14 47-2357-102-18 All lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.

device · product 5 of 8

ITST THREADED GUIDE PIN

Z-0589-2014
Recall number
Z-0589-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item Numbers: 47-2258-067-00 All Lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.

device · product 6 of 8

NGK Stem Ext 24 x 245mm

Z-0590-2014
Recall number
Z-0590-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item Numbers: 32-5988-012-24 All lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.

device · product 7 of 8

FEM COND BUTTRESS PLT, LT

Z-0591-2014
Recall number
Z-0591-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item #'s: 00-2347-002-12 00-2347-002-14 00-2347-002-16 00-2347-002-18 Lot #s: All lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.

device · product 8 of 8

TIB NAIL

Z-0592-2014
Recall number
Z-0592-2014
Initiated
November 05, 2013
Classification
Class II
Status
Terminated
Recalling firm
Zimmer, Inc.
Quantity
42, 065 units total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity. This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure

Code information

Item #'s: 32-8553-311-59 32-8553-311-61 32-8553-311-63 32-8553-311-65 Lot #s: All lots with an expiration date prior to July 24, 2023

Distribution pattern

Worldwide Distribution.