Reported Jan 1, 2025 · Ongoing

Medline brand, medical procedure convenience 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?

Medline brand, medical procedure convenience kits, labeled as

18 of 18 products

Products covered by this recall
Model / numberProduct as published
CDS982719XCRANIOTOMY
DYNJ21927QMVFF/FIBU #54-RF
DYNJ21927SMVFF/FIBU #54-RF
DYNJ61607ANEURO PEDIATRIC
DYNJ66419CCRANIOTOMY PACK
DYNJ69907LYMPHATIC BYPASS PACK
DYNJ69907ALYMPHATIC BYPASS PACK
DYNJ81934BHEAD AND NECK PACK - 51597
DYNJ82007AMAJOR CRANIOTOMY PACK
DYNJ82011ASPINE PACK
DYNJ84068CRANIOTOMY MERCY STK 256
DYNJ84496AWMC UNIVERSAL NEURO PACK
DYNJ85830SPINE PACK LF
DYNJ903566DAHT SPINE PACK
DYNJ909364ALAMINECTOMY SPINAL FUSION PACK
DYNJ909472DIEP
DYNJ910292AMBULATORY SINUS
DYNJ910292AAMBULATORY SINUS
Lot codes and dates

18 of 18 products

Products covered by this recall
#BarcodesProduct as published
11019845906453140198459064532CDS982719X, 10198459064531 (each), 40198459064532 (case), Lot Numbers: 24IBE288
21088994288553440889942885535UDI-DI: DYNJ21927Q, 10889942885534 (each), 40889942885535 (case), Lot Numbers: 21LBB957 21KBA966 21IBN569 21GBO771 20KBB297 20JBB045 20IBI973 20HBU423 20HBC730 20EBU633
31019532757623340195327576234UDI-DI: DYNJ21927S, 10195327576233 (each), 40195327576234 (case), Lot Numbers: 24GBQ357 24GBK331 24FBF951 24CBV435 24BBN342 24ABW268
41019348966573440193489665735UDI-DI: DYNJ61607A, 10193489665734 (each), 40193489665735 (case), Lot Numbers: 22FLB055 22FLA458
51019845905935340198459059354UDI-DI: DYNJ66419C, 10198459059353 (each), 40198459059354 (case), Lot Numbers: 24IBG439
61019348999555840193489995559UDI-DI: DYNJ69907, 10193489995558 (each), 40193489995559 (case), Lot Numbers: 22EMA026
71019532716397640195327163977UDI-DI: DYNJ69907A, 10195327163976 (each), 40195327163977 (case), Lot Numbers: 22FMB386
81019845912291040198459122911UDI-DI: DYNJ81934B, 10198459122910 (each), 40198459122911 (case), Lot Numbers: 24IBG522
91019532763546640195327635467UDI-DI: DYNJ82007A, 10195327635466 (each), 40195327635467 (case), Lot Numbers: 24IME319 24HMI978 24HMI081 24CMA496
101019532763548040195327635481UDI-DI: DYNJ82011A, 10195327635480 (each), 40195327635481 (case), Lot Numbers: 24HMI979 24GMJ808 24GMB190 24FMD601 24EMD223 24BMJ118
111019532733214340195327332144UDI-DI: DYNJ84068, 10195327332143 (each), 40195327332144 (case), Lot Numbers: 23HLA314
121019845901124540198459011246UDI-DI: DYNJ84496A, 10198459011245 (each), 40198459011246 (case), Lot Numbers: 24HBF172 24FBN697
131019532755647140195327556472UDI-DI: DYNJ85830, 10195327556471 (each), 40195327556472 (case), Lot Numbers: 24IBG585 24DBO636 24BBK513
141019532756082940195327560820UDI-DI: DYNJ903566D, 10195327560829 (each), 40195327560820 (case), Lot Numbers: 24BBO346 24BBK920 24ABO451 24ABO420
151019532766042040195327660421UDI-DI: DYNJ909364A, 10195327660420 (each), 40195327660421 (case), Lot Numbers: 24IMD666 24IMB155 24GMA069 24EMH357
161019532736882140195327368822UDI-DI: DYNJ909472, 10195327368821 (each), 40195327368822 (case), Lot Numbers: 24IMD560 24GMI069 23LMG055 23KMD713 23GME971 23GMA619
171019532761868140195327618682UDI-DI: DYNJ910292, 10195327618681 (each), 40195327618682 (case), Lot Numbers: 24HBI255 24HBF816 24GBR460 24FBL017
181019845911172340198459111724UDI-DI: DYNJ910292A, 10198459111723 (each), 40198459111724 (case), Lot Numbers: 24IBK954

This recall covers 17 products

The agency filed one notice per product. You are reading one of them; the other 16 are below.

4 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods

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, 5:37 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.