Reported Apr 10, 2024 · Ongoing

Centurion Curette 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 Curette kits labeled as

9 of 9 products

Products covered by this recall
Model / numberProduct as published
66745STERILE BUCK EAR CURETTE "00" (25697)
67050STERILE "1" EAR CURETTE (505629)
67430STERILE FOX DERMAL CURETTE, 5MM(32923)
I67970STERILE EXCAVATOR CURETTE (P/S)
I68040ST BUCK EAR CURETTE BLNT STR SZ 00
I68340STERILE BRUNS CURETTE #4 (BC400S)
I683806MM FOX DERMAL CURETTE STERILE
I68470STERILE KEVORKIAN CURETTE 4MM (KEC4S)
I68480ST ENDOCERVICAL BIOPSY CURETTE 2MM
Lot codes and dates

9 of 9 products

Products covered by this recall
#BarcodesProduct as published
1706531600603300065316006033166745, UDI/DI 70653160060330 (case) 00653160060331 (each), Lot Numbers: 2023103090
2006531603575091065316035750667050, UDI/DI 00653160357509 (case) 10653160357506 (each), Lot Numbers: 2023103090
3106531601235140065316012351767430, UDI/DI 10653160123514 (case) 00653160123517 (each), Lot Numbers: 2023022190
42065316022474400653160224740I67970, UDI/DI 20653160224744 (case) 00653160224740 (each), Lot Numbers: 2023041390, 2023041490, 2023061990, 2023101290
52065316022860500653160228601I68040, UDI/DI 20653160228605 (case) 00653160228601 (each), Lot Numbers: 2023022190, 2023102090
60065316027986310653160279860I68340, UDI/DI 00653160279863 (case) 10653160279860 (each), Lot Numbers: 2023042490
70065316028455310653160284550I68380, UDI/DI 00653160284553 (case) 10653160284550 (each), Lot Numbers: 2023032790, 2023101790
80065316029072110653160290728I68470, UDI/DI 00653160290721 (case) 10653160290728 (each), Lot Numbers: 2023032190, 2023032390
90065316029264010653160292647I68480, UDI/DI 00653160292640 (case) 10653160292647 (each), Lot Numbers: 2023013190
Amount recalled
20614 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:42 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.