Zimmer recalls specific surgical instruments due to possible use of incorrect materials. Affected items have 'Normed' marking; contact for details.
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
Zimmer is recalling certain surgical instruments that may have been made from the wrong material. This could affect the safety and performance of the tools during medical procedures.
The instruments might contain materials not specified in their design, which could lead to improper function during surgery. This may cause complications if the tools do not work as intended.
Surgical professionals using Zimmer's CBS micro, countersink, and cannulated instruments with 'Normed' markings are affected. Patients and medical staff are at risk if the instruments fail during procedures.
Check for the 'Normed' marking on the instrument. Affected items are part of Zimmer's CBS micro, countersink, cannulated, and AO series with Item Number 503004541.
Look for the 'Normed' marking on the instrument to determine if it is affected.
No, only specific instruments with 'Normed' markings and Item Number 503004541 are affected.
The recall record does not specify a remedy, so contact Zimmer directly for guidance.
The recall states a possible material issue but does not mention injury risks, so the risk level is low.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1460-2019 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1460-2019 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.
