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
26 of 26 products
| Model / number | Product as published |
|---|---|
66225 | STERILE TUBE OCCLUDING FORCEP (TO8256) |
66565 | ST. KELLY HEMO W/TIPS (SK8039) |
66810 | STERILE BUTTERFLY PROBE (P837) |
66900 | STERILE PROBE (PR5) |
67110 | STERILE NAIL NIPPER |
67285 | STERILE FREER SEPTUM ELEVATOR (FE75B) |
67365 | STERILE 5 1/2" NAIL NIPPER (32195) |
67420 | STERILE 4 1/4" CUTICLE NIPPER (32908) |
67595 | STERILE ENGLISH ANVIL NAIL SPLITTER-5" |
67780 | STERILE UNIVERSAL RING CUTTER(FS02470) |
589784ST | STERILE FINGER NAIL CLIPPER |
BEL46ST | BILLEAU EAR LOOP 4MM 6" LARGE |
DYND04011 | PROBE WITH EYE |
I67350 | STERILE 9" MAYO SCISSOR (ST150) |
I67695 | STRL ROCHESTER OCHSNER SATIN 7 1/4" |
I67980 | CMP* NAIL NIPPER ANGLED 4.5 |
I67995 | STERILE BILLEAU EAR LOOP 3MM |
I68020 | ST. ALLIGATOR FORCEP, POINTED, MICRO P/S |
I68190 | MOSQUITO HEMOSTAT FINE TIP |
I68200 | STERILE VAS DEFERENS CLAMP (VDC100S) |
- Lot codes and dates
26 of 26 products
Products covered by this recall # Barcodes Product as published 1 606531600183270065316001832566225, UDI/DI 60653160018327 (case) 00653160018325 (each), Lot Numbers: 2023070390 2 206531600598650065316005986166565, UDI/DI 20653160059865 (case) 00653160059861 (each), Lot Numbers: 2023022090 3 606531600385470065316003854566810, UDI/DI 60653160038547 (case) 00653160038545 (each), Lot Numbers: 2023042490 4 606531600388680065316003886666900, UDI/DI 60653160038868 (case) 00653160038866 (each), Lot Numbers: 2023030890, 2023100390, 2023111090 5 506531600497510065316004975667110, UDI/DI 50653160049751 (case) 00653160049756 (each), Lot Numbers: 2023042490, 2023051590, 2023110290 6 506531600891390065316008913467285, UDI/DI 50653160089139 (case) 00653160089134 (each), Lot Numbers: 2023081490, 2023101190 7 106531601151200065316011512367365, UDI/DI 10653160115120 (case) 00653160115123 (each), Lot Numbers: 2023040390, 2023090790, 2023101790, 2023110890 8 106531601234910065316012349467420, UDI/DI 10653160123491 (case) 00653160123494 (each), Lot Numbers: 2023100590 9 106531601845530065316018455667595, UDI/DI 10653160184553 (case) 00653160184556 (each), Lot Numbers: 2023032890, 2023101390 10 106531601966620065316019666567780, UDI/DI 10653160196662 (case) 00653160196665 (each), Lot Numbers: 2023071290 11 4065316013068100653160130683589784ST, UDI/DI 40653160130681 (case) 00653160130683 (each), Lot Numbers: 2023020990, 2023030790, 2023042890 12 1065316022716800653160227161BEL46ST, UDI/DI 10653160227168 (case) 00653160227161 (each), Lot Numbers: 2023101890 13 4088438909780010884389097809DYND04011, UDI/DI 40884389097800 (case) 10884389097809 (each), Lot Numbers: 2023102090 14 0065316028684710653160286844I67350, UDI/DI 00653160286847 (case) 10653160286844 (each), Lot Numbers: 2023031390, 2023111790 15 0065316026306010653160263067I67695, UDI/DI 00653160263060 (case) 10653160263067 (each), Lot Numbers: 2023110290 (not distributed) 16 1065316022481500653160224818I67980, UDI/DI 10653160224815 (case) 00653160224818 (each), Lot Numbers: 2023031690 17 1065316022765600653160227659I67995, UDI/DI 10653160227656 (case) 00653160227659 (each), Lot Numbers: 2023042690, 2023101790, 2023111090 18 1065316022834900653160228342I68020, UDI/DI 10653160228349 (case) 00653160228342 (each), Lot Numbers: 2023092990, 2023111590 19 0065316026329910653160263296I68190, UDI/DI 00653160263299 (case) 10653160263296 (each), Lot Numbers: 2023041390, 2023090790 20 0065316026307710653160263074I68200, UDI/DI 00653160263077 (case) 10653160263074 (each), Lot Numbers: 2023101890 - Amount recalled
- 60075 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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