Quick Facts at a Glance
- Recall Date
- December 24, 2025
- Hazard Level
- HIGH
- Brand
- Zimmer Surgical
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Zimmer Surgical
- Product type
- Tourniquet Systems
- Model numbers
- Lot Code: Model No. 60320010100, UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739001", Lot No. 67505739, Serial No. 32067505739001 Model No. 60320010100, UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739003", Serial No. 32067505739003 Model No. 60320010100, UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739004", Serial No. 32067505739004 Model No. 60320010100 +7 more
- Sold at
- Multiple Retailers
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 24, 2025
Reported by FDA DEVICE
February 4, 2026
RecallRadar source check
April 13, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
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
About This Product
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.
Why This Is Dangerous
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.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
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.
Practical Guidance
How to identify if yours is affected
- Check the model number is 60320010100.
- Verify the software version is v2.06 or prior.
- Look for the lot number 67505739 or serial numbers listed in the recall.
Where to find product info
The model number and software version can usually be found on the device's label or in the user manual.
What timeline to expect
Expect a processing timeline of approximately 4-6 weeks for refunds or replacements after following the recall instructions.
If the manufacturer is unresponsive
- Contact Zimmer Surgical Inc again via their customer service number.
- Document your correspondence attempts and provide this information in further communications.
How to prevent similar issues
- When purchasing medical devices, ensure they have the latest software updates.
- Check for recalls prior to use, especially for critical medical equipment.
- Choose devices from manufacturers known for responsive customer service.
Documentation advice
Keep a record of all communications regarding the recall, including emails, letters, and any responses from Zimmer Surgical Inc.
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Product Details
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.
Key Facts
- Recall date: December 24, 2025
- Software version: v2.06 or prior
- Total recalled units: 51
- International distribution: Canada and EMEA
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