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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79677

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

Open FDA event record

Event summary

Timeline bucket
February 28, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Zimmer GmbH

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

2 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 2

Avenir Muller Stem; Item Number: 01.06010.003, Lot Number: 2904368, UDI: (01) 00889024479494 (17) 220331 (10) 2904368

Z-1524-2018
Recall number
Z-1524-2018
Initiated
February 28, 2018
Classification
Class II
Status
Terminated
Recalling firm
Zimmer GmbH
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
A potential commingle that could result in the product in the package not matching the product on the outer label.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A potential commingle that could result in the product in the package not matching the product on the outer label.

Code information

Lot Number: 2904368

Distribution pattern

There was no distribution to the US. The distribution occurred to the following countries: Belgium, Switzerland, Germany, France, Canary Islands, Italy, and Thailand.

device · product 2 of 2

Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)220430 (10)2905496

Z-1525-2018
Recall number
Z-1525-2018
Initiated
February 28, 2018
Classification
Class II
Status
Terminated
Recalling firm
Zimmer GmbH
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
A potential commingle that could result in the product in the package not matching the product on the outer label.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A potential commingle that could result in the product in the package not matching the product on the outer label.

Code information

Lot Number: 2905496

Distribution pattern

There was no distribution to the US. The distribution occurred to the following countries: Belgium, Switzerland, Germany, France, Canary Islands, Italy, and Thailand.