Reported Apr 10, 2024 · Ongoing
Centurion Forcep 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 Forcep kits labeled as
26 of 26 products
| Model / number | Product as published |
|---|---|
66165 | STERILE F/P SPLINTER FORCEP (SF6141) |
66185 | STERILE WEBSTER NEEDLEHOLDER |
66195 | STERILE ADSON FORCEP SERR (598) |
66200 | STERILE DRESSING FORCEP SERR (DF6003) |
66205 | STERILE TISSUE FORCEP W/TEETH (TF6015) |
66220 | STERILE F/P WEBSTER NEEDLEHOLDER FN8064 |
66275 | STERILE IRIS FORCEP W/TEETH (IF250) |
66280 | STERILE TUBE CLAMP (TOC500) |
66355 | STERILE F/P SATIN NEEDLEHOLDER (FN9050S) |
66360 | STERILE 9 1/2 SPONGE FORCEP (237) |
66375 | STERILE SATIN NEEDLEHOLDER (FN6060S) |
66395 | STERILE CURV CRILE FORCEP (CF81810) |
66415 | STERILE LUCAE FORCEP (BF212) |
66430 | STERILE 6" SF MAYO NEEDLEHOLDER P/S |
66440 | STERILE SATIN FORCEP W/TEETH (AF058S) |
66470 | STERILE 6" FACIAL NEEDLEHOLDER (FN7070S) |
66490 | STERILE BAYONET FORCEP (25695) |
66500 | STERILE WEBSTER NEEDLEHOLDER (WN8080S) |
66510 | STERILE O-H NEEDLEHOLDER (OHN7098S) |
66515 | STERILE FEILCHENFELD FORCEP (FS388) |
- Lot codes and dates
30 of 30 products
Products covered by this recall # Barcodes Product as published 1 606531600183340065316001833266165, UDI/DI 60653160018334 (case) 00653160018332 (each), Lot Numbers: 2023111790 2 606531600048870065316000488566185, UDI/DI 60653160004887 (case) 00653160004885 (each), Lot Numbers: 2023041090, 2023072590, 2023120190 3 606531600066380065316000663666195, UDI/DI 60653160006638 (case) 00653160006636 (each), Lot Numbers: 2023042090, 2023053090, 2023090890, 2023111790 4 606531600226070065316002260566200, UDI/DI 60653160022607 (case) 00653160022605 (each), Lot Numbers: 2023020890 5 606531600319440065316003194266205, UDI/DI 60653160031944 (case) 00653160031942 (each), Lot Numbers: 2023030390 6 606531600248090065316002480766220, UDI/DI 60653160024809 (case) 00653160024807 (each), Lot Numbers: 2023111490 7 606531600388820065316003888066275, UDI/DI 60653160038882 (case) 00653160038880 (each), Lot Numbers: 2023060690 8 606531600048700065316000487866280, UDI/DI 60653160004870 (case) 00653160004878 (each), Lot Numbers: 2023113090 9 606531600232770065316002327566355, UDI/DI 60653160023277 (case) 00653160023275 (each), Lot Numbers: 2023042790 10 506531600223650065316002236066360, UDI/DI 50653160022365 (case) 00653160022360 (each), Lot Numbers: 2023032090 11 606531600048560065316000485466375, UDI/DI 60653160004856 (case) 00653160004854 (each), Lot Numbers: 2023032790, 2023112990, 2023113090 12 606531600440360065316004403466395, UDI/DI 60653160044036 (case) 00653160044034 (each), Lot Numbers: 2023071890 13 606531600188150065316001881366415, UDI/DI 60653160018815 (case) 00653160018813 (each), Lot Numbers: 2023041390, 2023101390 14 206531600412110065316004121766430, UDI/DI 20653160041211 (case) 00653160041217 (each), Lot Numbers: 2023032390 15 706531600223520065316002235366440, UDI/DI 70653160022352 (case) 00653160022353 (each), Lot Numbers: 2023100990, 2023102790 16 106531600393890065316003938266470, UDI/DI 10653160039389 (case) 00653160039382 (each), Lot Numbers: 2023070390 17 106531600090300065316000903366490, UDI/DI 10653160009030 (case) 00653160009033 (each), Lot Numbers: 2023021690 18 606531600438480065316004384666500, UDI/DI 60653160043848 (case) 00653160043846 (each), Lot Numbers: 2023031090 19 106531600505200065316005052366510, UDI/DI 10653160050520 (case) 00653160050523 (each), Lot Numbers: 2023071290 20 606531600409530065316004095166515, UDI/DI 60653160040953 (case) 00653160040951 (each), Lot Numbers: 2023041090, 2023071290, 2023111590 - Amount recalled
- 274410 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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