Zimmer recalls A.T.S. 3200TS Tourniquet Systems with software version v2.06 or earlier that may freeze in non-English language settings, causing delays when locating an alternate device.
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
Zimmer is recalling A.T.S. 3200TS Tourniquet Systems with software version v2.06 or earlier. These devices may freeze or become unresponsive to touch when used in non-English language settings, potentially causing delays while searching for an alternate device.
The device's screen may freeze or become unresponsive to touch when operating in non-English language settings. This could cause delays while searching for an alternate device during medical procedures.
Medical professionals using Zimmer A.T.S. 3200TS Tourniquet Systems with software version v2.06 or earlier are most at risk. This recall affects specific model numbers and serial numbers listed in the recall notice.
Check for model number 60320010100 with software version v2.06 or earlier. Look for specific serial numbers and lot codes listed in the recall notice.
Verify the software version on your device; versions v2.06 or earlier are affected.
No, but you should check the software version. If it's v2.06 or earlier, you may need to take action.
The recall states that the screen may freeze in non-English settings, but this is not an immediate safety hazard. Check the software version first.
Check for model number 60320010100 with software version v2.06 or earlier. Specific serial numbers and lot codes are listed in the recall notice.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1202-2026 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1202-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
