Zimmer recalls two hip implant models with incorrect size labeling. This mix-up could lead to improper fit if used, but no injuries reported. Affected units include specific item numbers and lot numbers.
The outer package labeling and product etch are for a Size 6, however, the implant is a Size 4, and vice versa.
Zimmer is recalling hip implants that have the wrong size labeled on them. Using these could cause improper fit and potential complications during surgery or recovery.
The packaging and product labels indicate the wrong size implant. For example, a Size 4 implant is labeled as Size 6, and vice versa. This mix-up could lead to improper fit during surgery or recovery.
Patients who received the recalled hip implants (Size 4 or Size 6) are most at risk. Healthcare providers who use these implants for surgery may also be affected.
Check the item number on the implant: 00771100640 (Size 4) or 00771100440 (Size 6). Also look for the lot number: 65236202 or 65249215.
Verify the implant size by checking the item number and lot number on the packaging or implant itself.
The recall record does not mention any injuries.
Check the item number: 00771100640 (Size 4) or 00771100440 (Size 6), and lot number: 65236202 or 65249215.
The recall record does not specify a return or remedy action.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-2519-2023 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-2519-2023 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.
