Fresh Recalls

FDAClass II · Medical device · Recall Z-1993-2026 · Recalled May 6, 2026

Depuy Synthes recall — DEPUY (IRELAND)

Agency report date: May 6, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Depuy Synthes
Company / brand
DEPUY (IRELAND)
Lot / serial / date codes
Part Number: 150450208. UDI-DI: 10603295543039. Lot Numbers: AF1008441, AF1008028. Expiration Date: 12/31/2035.
Distribution
US Nationwide distribution in the states of MN, NC, TX.
Agency product description and boundaries

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Depuy Synthes recall status

3. Open the official notice or contact

Official recall ID
Z-1993-2026
Brand
All DEPUY (IRELAND) recalls
Classification
Class II
Units affected
3 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Co. Cork, Ireland
Firm address
Loughbeg, Ringaskiddy, N/A

Identifying details (verbatim from the notice)

Product codes / lots
Part Number: 150450208. UDI-DI: 10603295543039. Lot Numbers: AF1008441, AF1008028. Expiration Date: 12/31/2035.
Distribution
US Nationwide distribution in the states of MN, NC, TX.
Firm notified the public via
E-Mail
FDA event ID
98707
Recall initiated
April 3, 2026
FDA classified
April 29, 2026
FDA report date
May 6, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved August 4, 2026 at 11:00 PM UTC.

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