Zimmer recalls A.T.S. 5000TS Tourniquet Systems with software version v2.04 or older that may freeze or become unresponsive in non-English language settings, causing delays in finding alternate devices.
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. 5000TS Tourniquet Systems with software version v2.04 or older that may freeze or become unresponsive when used in non-English language settings. This could delay finding an alternate device during use, but it does not pose a risk of injury.
The device's screen may freeze or become unresponsive to touch when operating in non-English language settings. This could cause delays while the user searches for an alternate device, but it does not cause injury or damage.
Medical professionals using these tourniquet systems in non-English language settings may experience delays when the device screen freezes. The risk is minimal and does not involve injury.
Check for software version v2.04 or older on the A.T.S. 5000TS Tourniquet Systems. Model number 60500010100 with specific serial numbers and lot codes listed in the recall details.
Verify the software version on your device; if it is v2.04 or older, it is affected.
Yes, if your A.T.S. 5000TS Tourniquet System has software version v2.04 or older, it is affected.
Check the software version on your device; affected units have version v2.04 or older.
The recall does not specify a fix; the remedy is null 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-1201-2026 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1201-2026 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.
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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.
