Zimmer recalls Z1 Femoral Hip System (Product #611777612) due to potential stem inserter fracturing. Affected units include specific lot numbers and UDI-DI codes. Contact Zimmer for details.
There is a potential design issue with the Z1 Offset Stem Inserter leading to fracturing of the distal tip.
Zimmer is recalling a specific hip implant model because the stem inserter might break, causing injury. This affects patients who received the product with the listed lot numbers. Immediate action is needed to prevent harm.
The Z1 Offset Stem Inserter could fracture under normal use, potentially causing the hip implant to become unstable. This might lead to pain, dislocation, or the need for additional surgery.
Patients who received the Z1 Femoral Hip System with the listed lot numbers (102646, 102777, etc.) are most at risk. Medical professionals who used this product during surgery may also be affected.
Check the product's lot numbers: 102646, 102777, 102778, 104095, 104324, or 105277. Also look for the UDI-DI code 00887868577888 on the packaging.
Identify your lot numbers and UDI-DI code to confirm if your Z1 Femoral Hip System is affected.
Reach out to Zimmer directly for further instructions on next steps.
Yes, the Z1 Offset Stem Inserter has a potential design issue that could cause fracturing of the distal tip, leading to instability or injury.
Check the lot numbers: 102646, 102777, 102778, 104095, 104324, or 105277. Also look for the UDI-DI code 00887868577888 on the packaging.
Contact Zimmer directly for specific instructions on next steps, as the recall remedy is not specified in the record.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1329-2025 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1329-2025 from Zimmer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
