Reported Jul 8, 2026 · Ongoing · Updated Sep 16, 2026

Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S� 4000 TS Tourniquet Systems Single Hose with CPC Connectors…

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 NameSterile
  • Tourniquet Hoses Product NameA.T.S� 4000 TS Tourniquet Systems Single Hose with
  • CPC Connectors Model/Catalog Number60-4009-101-00
  • Software VersionN/A
  • Product DescriptionSingle Sterile Extension
  • Hose with PLC Connector ComponentN/A
Lot codes and dates

37 of 37 products

Products covered by this recall
Model / numberBarcodesProduct as published
60-4009-101-00Lot Code
00889024382336Case (20-pack) UDI (01)00889024382336(17)271022(10)79701946
00889024380455Box (10-Pack) UDI (01)00889024380455(17)271022(10)79701946
00889024376786Individual UDI (01)00889024376786(17)271022(10)79701946
60-4009-101-00Lot Number 79701946
00889024382336Case (20-pack) UDI (01)00889024382336(17)271028(10)79701947
00889024380455Box (10-Pack) UDI (01)00889024380455(17)271028(10)79701947
00889024376786Individual UDI (01)00889024376786(17)271028(10)79701947
60-4009-101-00Lot Number 79701947
00889024382336Case (20-pack) UDI (01)00889024382336(17)271030(10)79701948
00889024380455Box (10-Pack) UDI (01)00889024380455(17)271030(10)79701948
00889024376786Individual UDI (01)00889024376786(17)271030(10)79701948
60-4009-101-00Lot Number 79701948
00889024382336Case (20-pack) UDI (01)00889024382336(17)280325(10)80555938
00889024380455Box (10-Pack) UDI (01)00889024380455(17)280325(10)80555938
00889024376786Individual UDI (01)00889024376786(17)280325(10)80555938
60-4009-101-00Lot Number 80555938
00889024382336Case (20-pack) UDI (01)00889024382336(17)280402(10)80555939
00889024380455Box (10-Pack) UDI (01)00889024380455(17)280402(10)80555939
00889024376786Individual UDI (01)00889024376786(17)280402(10)80555939
Amount recalled
14360

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.

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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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 5:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.