Reported Apr 23, 2025 · Ongoing

Medline Convenience kits used for various procedures

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 Convenience kits used for various procedures

15 of 15 products

Products covered by this recall
Model / numberProduct as published
DYNJ69733STANDARD D&C
DYNJ39904ANHS - LAP BOWEL GNG
DYNJ64651ALAPAROSCOPY GYN SURGERY PA
DYNJ49250FGYNE - LITHOTOMY MAJOR-LF
DYNJ47552CENS. GYNE LITHOMIE MINEURE-LF
DYNJ67945CH D&C PACK
DYNJ25892KLAP GYN PACK-LF
DYNJ41670BGYN LAPAROSCOPY PACK BJC-LF
DYNJ67227OPP GYN VAGINAL PACK
DYNJ41790FGYNE MINOR LAPAROSCOPY GRH-LF
DYNJ49251CGYNE - LITHOTOMY MINOR PACK-LF
DYNJ69733STANDARD D&C
DYNJ24338IPERI GYN PACK
CDS982727LGYN LAPAROSCOPY CDS
DYNJ908712BROBOTICS
Lot codes and dates

15 of 15 products

Products covered by this recall
#BarcodesProduct as published
11088827780190540888277801906Lot Number: 24IBE079; 2) DYNJ39904A, UDI-DI: 10888277801905(each), 40888277801906(case)
21019532705738140195327057382Lot Number: 24IBF466; 3) DYNJ64651A, UDI-DI: 10195327057381(each), 40195327057382(case)
31019532768014540195327680146Lot Number: 24IBS312; 4) DYNJ49250F, UDI-DI: 10195327680145(each), 40195327680146(case)
41019348984559440193489845595Lot Number: 24JBM609; 5) DYNJ47552C, UDI-DI: 10193489845594(each), 40193489845595(case)
51019348945869540193489458696Lot Number: 24JBN271; 6) DYNJ67945, UDI-DI: 10193489458695(each), 40193489458696(case)
61019348990543440193489905435Lot Number: 24JBU691; 7) DYNJ25892K, UDI-DI: 10193489905434(each), 40193489905435(case)
71019845912422840198459124229Lot Number: 24JBV586; 8) DYNJ41670B, UDI-DI: 10198459124228(each), 40198459124229(case)
81019348939164040193489391641Lot Number: 24KBA786; 9) DYNJ67227, UDI-DI: 10193489391640(each), 40193489391641(case)
91019532754713440195327547135Lot Number: 24KBC196; 10) DYNJ41790F, UDI-DI: 10195327547134(each), 40195327547135(case)
101019532767964440195327679645Lot Number: 24KBC471; 11) DYNJ49251C, UDI-DI: 10195327679644(each), 40195327679645(case)
111019348997408940193489974080Lot Number: 24KBG007; 12) DYNJ69733, UDI-DI: 10193489974089(each), 40193489974080(case)
121019348932616140193489326162Lot Number: 24KBH831; 13) DYNJ24338I, UDI-DI: 10193489326161(each), 40193489326162(case)
131019532725802340195327258024Lot Number: 24KBH862; 14) CDS982727L, UDI-DI: 10195327258023(each), 40195327258024(case)
141019845918721640198459187217Lot Number: 24KBU700; 15) DYNJ908712B, UDI-DI: 10198459187216(each), 40198459187217(case)
15Lot Number: 24LBF830
Amount recalled
706 units

This recall covers 34 products

The agency filed one notice per product. You are reading one of them; the other 33 are below.

21 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

This product could cause temporary or reversible health problems — stop using it.

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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, 7:38 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.