Zimmer Surgical recalled 51 A.T.S. 3200TS Tourniquet Systems on December 24, 2025, due to a malfunctioning user interface. The device may freeze or become unresponsive in non-English language settings, risking delays in emergency situations. Healthcare providers should stop using the device immediately and follow recall instructions.
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.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Zimmer Surgical Inc or your healthcare provider for instructions. Notification method: Letter
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The A.T.S. 3200TS Tourniquet Systems are designed for emergency medical situations, providing compression to control bleeding. Healthcare professionals utilize these devices during trauma care to stabilize patients effectively.
The device may freeze or become unresponsive, particularly in non-English language settings, which can prevent timely medical intervention. This malfunction could result in significant delays when immediate action is necessary.
This recall is not part of a broader industry pattern.
The recall requires healthcare providers to stop using the device, which could lead to operational delays and the need for alternative solutions in emergency settings.
The model number and software version can usually be found on the device's label or in the user manual.
Expect a processing timeline of approximately 4-6 weeks for refunds or replacements after following the recall instructions.
Keep a record of all communications regarding the recall, including emails, letters, and any responses from Zimmer Surgical Inc.
The recalled product is the A.T.S. 3200TS Tourniquet Systems, model number 60320010100, with software version v2.06 or prior. It was distributed internationally to Canada and EMEA countries. The price of the product is not specified.
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