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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 88304

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

Open FDA event record

Event summary

Timeline bucket
June 02, 2021
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Biomet, 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

17 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 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size A, 50 MM Item Number: 11-301300

Z-2259-2021
Recall number
Z-2259-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
88 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 626440 (01)00880304474611(17)310409(10)626440 626450 (01)00880304474611(17)310322(10)626450 626460 (01)00880304474611(17)310402(10)626460 626890 (01)00880304474611(17)310323(10)626890 678370 (01)00880304474611(17)310419(10)678370 678770 (01)00880304474611(17)310419(10)678770 678800 (01)00880304474611(17)310409(10)678800 695830 (01)00880304474611(17)310412(10)695830

Distribution pattern

US Nationwide distribution.

device · product 2 of 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size A, 60 MM Item Number: 11-301301

Z-2260-2021
Recall number
Z-2260-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : Lot Number UDI Number 626490 (01)00880304468030(17)310412(10)626490 679210 (01)00880304468030(17)310418(10)679210

Distribution pattern

US Nationwide distribution.

device · product 3 of 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size B, 60 MM Item Number: 11-301302

Z-2261-2021
Recall number
Z-2261-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
21 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 626540 (01)00880304474123(17)310423(10)626540 679320 (01)00880304474123(17)310419(10)679320

Distribution pattern

US Nationwide distribution.

device · product 4 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size A, 50 MM Item Number: 11-301310

Z-2262-2021
Recall number
Z-2262-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
81 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 004230 (01)00880304473799(17)310412(10)004230 626590 (01)00880304473799(17)310312(10)626590 626600 (01)00880304473799(17)310314(10)626600 678840 (01)00880304473799(17)310305(10)678840 679170 (01)00880304473799(17)310423(10)679170 679180 (01)00880304473799(17)310318(10)679180 880170 (01)00880304473799(17)310409(10)880170

Distribution pattern

US Nationwide distribution.

device · product 5 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size A, 60 MM Item Number: 11-301311

Z-2263-2021
Recall number
Z-2263-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
22 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 678930 (01)00880304474086(17)310315(10)678930 880200 (01)00880304474086(17)310427(10)880200

Distribution pattern

US Nationwide distribution.

device · product 6 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size B, 60 MM Item Number: 11-301312

Z-2264-2021
Recall number
Z-2264-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
33 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 678950 (01)00880304474093(17)310416(10)678950 880250 (01)00880304474093(17)310422(10)880250 880790 (01)00880304474093(17)310331(10)880790

Distribution pattern

US Nationwide distribution.

device · product 7 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size D, 60 MM Item Number: 11-301314

Z-2265-2021
Recall number
Z-2265-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
10 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 934870 (01)00880304474024(17)310419(10)934870

Distribution pattern

US Nationwide distribution.

device · product 8 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size E, 60 MM Item Number: 11-301315

Z-2266-2021
Recall number
Z-2266-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
7 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 626180 (01)00880304480551(17)310414(10)626180

Distribution pattern

US Nationwide distribution.

device · product 9 of 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size A, 70 MM Item Number: 11-301321

Z-2267-2021
Recall number
Z-2267-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
11 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 881730 (01)00880304474314(17)310324(10)881730

Distribution pattern

US Nationwide distribution.

device · product 10 of 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size B, 70 MM Item Number: 11-301322

Z-2268-2021
Recall number
Z-2268-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
11 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 678990 (01)00880304473751(17)310407(10)678990

Distribution pattern

US Nationwide distribution.

device · product 11 of 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM Item Number:11-301325

Z-2269-2021
Recall number
Z-2269-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
11 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 880850 (01)00880304480575(17)310412(10)880850

Distribution pattern

US Nationwide distribution.

device · product 12 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size A, 70 MM Item Number: 11-301331

Z-2270-2021
Recall number
Z-2270-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 880380 (01)00880304474628(17)310420(10)880380 880870 (01)00880304474628(17)310406(10)880870

Distribution pattern

US Nationwide distribution.

device · product 13 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size C, 70 MM Item Number: 11-301333

Z-2271-2021
Recall number
Z-2271-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
12 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 696800 (01)00880304474260(17)310504(10)696800

Distribution pattern

US Nationwide distribution.

device · product 14 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size E, 70 MM Item Number: 11-301335

Z-2272-2021
Recall number
Z-2272-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 881130 (01)00880304480483(17)310418(10)881130

Distribution pattern

US Nationwide distribution.

device · product 15 of 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size B, 80 MM Item Number: 11-301342

Z-2273-2021
Recall number
Z-2273-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
12 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 391390 (01)00880304474208(17)310323(10)391390

Distribution pattern

US Nationwide distribution.

device · product 16 of 17

Arcos Modular Revision Hip System Standard Cone Prox Body, Size C, 80 MM Item Number: 11-301343

Z-2274-2021
Recall number
Z-2274-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 626750 (01)00880304474499(17)310415(10)626750

Distribution pattern

US Nationwide distribution.

device · product 17 of 17

Arcos Modular Revision Hip System High Offset Cone Prox Body, Size D, 80 MM Item Number: 11-301354

Z-2275-2021
Recall number
Z-2275-2021
Initiated
June 02, 2021
Classification
Class II
Status
Terminated
Recalling firm
Biomet, Inc.
Quantity
12 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention

Code information

Lot Numbers/UDI : 880960 (01)00880304474307(17)310504(10)880960

Distribution pattern

US Nationwide distribution.