Reported Feb 4, 2026 · Ongoing
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100…
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.¿ 5000TS
- Tourniquet Systems Model/Catalog Number60500010100
- Software VersionSoftware version v2.04 or prior are within scope of the recall for A.T.S.¿ 5000TS
- Product DescriptionA.T
- S 5000TS Tourniquet Systems ComponentN/A
- Lot codes and dates
619 of 619 products
Products covered by this recall Model / number Barcodes Product as published 60500010100Lot Code — 0088902462645450066722609001UDI (01)00889024626454(11)240410(10)66722609(21)50066722609001 — Lot No. 66722609 6050001010050066722609001Serial No. 50066722609001 — 0088902462645450066722609002UDI "(01)00889024626454(11)240410(10)66722609(21)50066722609002 — Lot No. 66722609 6050001010050066722609002Serial No. 50066722609002 — 0088902462645450066722609003UDI "(01)00889024626454(11)240410(10)66722609(21)50066722609003" — Lot No. 66722609 6050001010050066722609003Serial No. 50066722609003 — 0088902462645450066722609004UDI "(01)00889024626454(11)240410(10)66722609(21)50066722609004" — Lot No. 66722609 6050001010050066722609004Serial No. 50066722609004 — 0088902462645450066722609005UDI "(01)00889024626454(11)240410(10)66722609(21)50066722609005" — Lot No. 66722609 6050001010050066722609005Serial No. 50066722609005 — 0088902462645450066722610001UDI "(01)00889024626454(11)240410(10)66722610(21)50066722610001" — Lot No. 66722610 6050001010050066722610001Serial No. 50066722610001 — 0088902462645450066722610002UDI "(01)00889024626454(11)240410(10)66722610(21)50066722610002" - Amount recalled
- 206
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.
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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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