Reported Apr 10, 2024 · Ongoing
Centurion Clamp kits labeled as
MEDLINE INDUSTRIES, LP - Northfield
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: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Centurion Clamp kits labeled as
6 of 6 products
| Model / number | Product as published |
|---|---|
66520 | STERILE BACKHAUS TOWEL CLAMP (BTC173) |
A547ST | STERILE TOWEL CLAMP |
I68080 | ST TOWEL CLAMPS NON PERFORATING (P/S) |
I68085 | STERILE TOWEL CLAMPS 5 1/2 |
I68095 | STERILE TOWEL CLAMPS 5 1/2" |
ZC110ST | ZIPSER PENIS CLAMP STERILE (ZC110) |
- Lot codes and dates
6 of 6 products
Products covered by this recall # Barcodes Product as published 1 606531600409600065316004096866520, UDI/DI 60653160040960 (case) 00653160040968 (each), Lot Numbers: 2023111590 2 1065316011368300653160113686A547ST, UDI/DI 10653160113683 (case) 00653160113686 (each), Lot Numbers: 2023020990, 2023033090, 2023060790, 2023092990 3 2065316023260200653160232608I68080, UDI/DI 20653160232602 (case) 00653160232608 (each), Lot Numbers: 2023072790 4 3065316023261600653160232615I68085, UDI/DI 30653160232616 (case) 00653160232615 (each), Lot Numbers: 2023032290, 2023071790 5 2065316023269500653160232691I68095, UDI/DI 20653160232695 (case) 00653160232691 (each), Lot Numbers: 2023062690 6 0065316025846210653160258469ZC110ST, UDI/DI 00653160258462 (case) 10653160258469 (each), Lot Numbers: 2023022490, 2023041090, 2023052290, 2023062890 - Amount recalled
- 12980 units
This recall covers 30 products
The agency filed one notice per product. You are reading one of them; the other 29 are below.
17 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
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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