Reported Feb 4, 2026 · Ongoing
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100…
Zimmer Surgical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Zimmer Surgical Inc · 200 W Ohio Ave · Dover, OH · 44622-9642
Is this the product you have?
- Brand NameZimmer
- Tourniquet Systems Product NameA.T.S.¿ 3200TS
- Tourniquet Systems Model/Catalog Number60320010100
- Software VersionSoftware version v2.06 or prior are within scope of the recall for A.T.S.¿ 3200TS
- Product DescriptionA.T
- S 3200TS Tourniquet Systems ComponentN/A
- Lot codes and dates
154 of 154 products
Products covered by this recall Model / number Barcodes Product as published 60320010100Lot Code — 0088902462644732067505739001UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739001" — Lot No. 67505739 6032001010032067505739001Serial No. 32067505739001 — 0088902462644732067505739003UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739003" — Lot No. 67505739 6032001010032067505739003Serial No. 32067505739003 — 0088902462644732067505739004UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739004" — Lot No. 67505739 6032001010032067505739004Serial No. 32067505739004 — 0088902462644732067505739005UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739005" — Lot No. 67505739 6032001010032067505739005Serial No. 32067505739005 — 0088902462644732067505739006UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739006" — Lot No. 67505739 6032001010032067505739006Serial No. 32067505739006 — 0088902462644732067505739007UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739007" — Lot No. 67505739 6032001010032067505739007Serial No. 32067505739007 — 0088902462644732067505739008UDI "(01)00889024626447(11)250725(10)67505739(21)32067505739008" - Amount recalled
- 51
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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