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 |
|---|---|
66580 | ST. VIRTUS SPLINTER FORCEP 6" (SF8246) |
I86630 | DEBRIDEMENT TRAY |
I86690 | BIOPSY INSTRUMENT PACK |
I86815 | DEBRIDEMENT TRAY |
MNS12675 | IR ADSON FORCEP & NEEDLE HOLDER |
DYNDA2346A | TOENAIL REMOVAL KIT, Product Code SUT20350 MEDLINE GENERAL PURPOSE INST. TRAY |
- Lot codes and dates
6 of 6 products
Products covered by this recall # Barcodes Product as published 1 106531600289630065316002896666580, UDI/DI 10653160028963 (case) 00653160028966 (each), Lot Numbers: 2023041090 2 0065316028654010653160286547I86630, UDI/DI 00653160286540 (case) 10653160286547 (each), Lot Numbers: 2023101190 3 0065316029075210653160290759I86690, UDI/DI 00653160290752 (case) 10653160290759 (each), Lot Numbers: 2023103190 4 0065316034229110653160342298I86815, UDI/DI 00653160342291 (case) 10653160342298 (each), Lot Numbers: 2023112190 5 0065316033734110653160337348MNS12675, UDI/DI 00653160337341 (case) 10653160337348 (each), Lot Numbers: 2023070390 6 00653160306552106531603065592019348919158210193489191585SUT20350, UDI/DI 00653160306552 (case) 10653160306559 (each), Lot Numbers: 2023022290, 2023041190, 2023042490, 2023052390, 2023101890 MEDLINE: UDI/DI 20193489191582 (case) 10193489191585 (each), Lot Numbers: 2023062290, 2023081490 - Amount recalled
- 7950 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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