Turbett Surgical recalls TS1200 sterilization containers due to potential weld failures that could breach sterile barriers, risking infection or injury during medical procedures.
Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries.
Turbett Surgical is recalling TS1200 sterilization containers because they might have weld failures that break the sterile barrier. This could lead to using unsterile instruments and cause infections or serious injuries during medical procedures.
The containers may develop weld failures that breach the sterile barrier. This allows unsterile instruments to be used, increasing the risk of infection or other serious injuries during medical procedures.
Healthcare providers using these containers for sterilizing medical devices are most at risk. Patients undergoing procedures with contaminated instruments could be affected.
Check for Turbett Surgical TS1200 containers with any lot or serial number. These containers are used for sterilizing medical devices and were sold to healthcare providers.
Inspect the container for signs of weld failures that might breach the sterile barrier.
The containers may have weld failures that breach the sterile barrier, leading to the use of unsterile instruments and potential infections or injuries.
Check for weld failures that might breach the sterile barrier. If you find issues, stop using it immediately and contact Turbett Surgical.
All lot numbers and serial numbers are affected as the recall covers all units.
We’ve drafted a message you can send Turbett Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1037-2023 — Turbett Surgical Turbett Surgical Hello, I own a Turbett Surgical that is covered by recall Z-1037-2023 from Turbett Surgical. 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.
