Zimmer recalls A.T.S 4000 TS Tourniquet Systems Dual Hose with CPC Connectors due to potential sterility breach in sealing area, which may cause moderate localized infection if used.
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.
Zimmer is recalling A.T.S 4000 TS Tourniquet Systems Dual Hose with CPC Connectors because of a potential sterility breach in the sealing area. If used, this could lead to moderate localized infection. If discovered before use, it might require extending surgery time to find an alternative device.
The sealing area of the sterile pouch may have a potential sterility breach. If used during surgery, this could lead to moderate localized infection. If discovered before use, it might require extending surgery time to find an alternative device.
Medical professionals using the A.T.S 4000 TS Tourniquet Systems Dual Hose with CPC Connectors for surgery. Those most at risk are surgeons and surgical teams handling the recalled product.
Look for the model number 60-1812-101-00 on the product. The product was sold in cases of 20 or 10 packs with specific lot numbers (e.g., 78938271, 80555986, etc.).
Identify the model number 60-1812-101-00 and lot numbers listed in the recall notice.
If discovered before use, it may result in clinically insignificant extension of surgery to find another readily available device. If used, it may cause moderate localized infection.
Look for the model number 60-1812-101-00 and specific lot numbers (e.g., 78938271, 80555986, etc.) on the product packaging.
The recall does not specify a remedy, so you should check with Zimmer Surgical Inc for further instructions.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-2673-2026 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-2673-2026 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.
