Reported Apr 10, 2024 · Ongoing
Centurion Manual surgical 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 Manual surgical kits labeled as
6 of 6 products
| Model / number | Product as published |
|---|---|
65140 | STERILE S/B WIRE SCISSOR |
65840 | SHARP/SHARP SCISSORS 41/2" |
66240 | STERILE WIRE CUTTER (WCS144) |
66855 | STERILE LISTER BANDAGE SCISSOR (LS122) |
67225 | STERILE UTILITY SHEARS (USH176) |
TRI66670 | STERILE ANGLED BANDAGE SCISSOR (LIST55) |
- Lot codes and dates
6 of 6 products
Products covered by this recall # Barcodes Product as published 1 606531600083800065316000838865140, UDI/DI 60653160008380 (case) 00653160008388 (each), Lot Numbers: 2023060790, 2023101090 2 606531600102080065316001020665840, UDI/DI 60653160010208 (case) 00653160010206 (each), Lot Numbers: 2023022790, 2023041190 3 606531600087930065316000879166240, UDI/DI 60653160008793 (case) 00653160008791 (each), Lot Numbers: 2023112790 4 506531600071880065316000718366855, UDI/DI 50653160007188 (case) 00653160007183 (each), Lot Numbers: 2023022490, 2023041990, 2023102690 5 506531600017660065316000176167225, UDI/DI 50653160001766 (case) 00653160001761 (each), Lot Numbers: 2023031690, 2023111490 6 1065316031797520653160317972TRI66670, UDI/DI 10653160317975 (case) 20653160317972 (each), Lot Numbers: 2023031490, 2023040690, 2023041090, 2023062790, 2023062890, 2023072490, 2023101690, 2023110190, 2023110990 - Amount recalled
- 84224 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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