Data Foundry

Medical device recalls 2026

Brand Name: Zimmer Tourniquet Systems Product Name: A — Class II medical device recall Z-1202-2026

Ongoing recall by Zimmer Surgical Inc, reported 2026-02-04. Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-Englis

Recall numberZ-1202-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmZimmer Surgical Inc, Dover, OH, United States
Recall initiated2025-12-24
Classified2026-01-28
Reported by FDA2026-02-04
Countries outside the USCA
Quantity51
UPC / GTIN / UDI-DI00889024626447, 32067505739001, 32067508816006, 32067508816013, 32067508816020, 32067508820003, 32067508820010
Lot numbers67505739, 67508816, 67508820
Serial numbers32067505739001, 32067505739003, 32067505739004, 32067505739005, 32067505739006, 32067505739007, 32067505739008, 32067505739010, 32067505739013, 32067505739014, 32067505739015, 32067505739017, 32067505739019, 32067505739020, 32067508816001, 32067508816002, 32067508816003, 32067508816004, 32067508816005, 32067508816006, 32067508816007, 32067508816008, 32067508816009, 32067508816010, 32067508816012 and 26 more
Model numbers60320010100

Product

Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are within scope of the recall for A.T.S.¿ 3200TS Product Description: A.T.S 3200TS Tourniquet Systems Component: N/A

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1202-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.