- Recalling firm
- DEPUY (IRELAND)
- Reason for recall
- The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
- Affected products (lot / model / serial)
- Part Number: 150450203. UDI-DI: 10603295533146. Lot Number: 1007537. Expiration Date: 10/31/2035.
- Units affected
- 3 units
- Distribution pattern
- US Nationwide distribution in the states of MN, NC, TX.
- Firm location
- Co. Cork, Ireland
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1989-2026
- Recall initiated
- April 3, 2026
- FDA classification date
- April 29, 2026
- FDA report date
- May 6, 2026
- FDA event ID
- 98707
- Last updated on HTM Vibe
- July 24, 2026