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
| Model / number | Product as published |
|---|---|
DYNJ69733 | STANDARD D&C |
DYNJ39904A | NHS - LAP BOWEL GNG |
DYNJ64651A | LAPAROSCOPY GYN SURGERY PA |
DYNJ49250F | GYNE - LITHOTOMY MAJOR-LF |
DYNJ47552C | ENS. GYNE LITHOMIE MINEURE-LF |
DYNJ67945 | CH D&C PACK |
DYNJ25892K | LAP GYN PACK-LF |
DYNJ41670B | GYN LAPAROSCOPY PACK BJC-LF |
DYNJ67227 | OPP GYN VAGINAL PACK |
DYNJ41790F | GYNE MINOR LAPAROSCOPY GRH-LF |
DYNJ49251C | GYNE - LITHOTOMY MINOR PACK-LF |
DYNJ69733 | STANDARD D&C |
DYNJ24338I | PERI GYN PACK |
CDS982727L | GYN LAPAROSCOPY CDS |
DYNJ908712B | ROBOTICS |
- Lot codes and dates
15 of 15 products
Products covered by this recall # Barcodes Product as published 1 1088827780190540888277801906Lot Number: 24IBE079; 2) DYNJ39904A, UDI-DI: 10888277801905(each), 40888277801906(case) 2 1019532705738140195327057382Lot Number: 24IBF466; 3) DYNJ64651A, UDI-DI: 10195327057381(each), 40195327057382(case) 3 1019532768014540195327680146Lot Number: 24IBS312; 4) DYNJ49250F, UDI-DI: 10195327680145(each), 40195327680146(case) 4 1019348984559440193489845595Lot Number: 24JBM609; 5) DYNJ47552C, UDI-DI: 10193489845594(each), 40193489845595(case) 5 1019348945869540193489458696Lot Number: 24JBN271; 6) DYNJ67945, UDI-DI: 10193489458695(each), 40193489458696(case) 6 1019348990543440193489905435Lot Number: 24JBU691; 7) DYNJ25892K, UDI-DI: 10193489905434(each), 40193489905435(case) 7 1019845912422840198459124229Lot Number: 24JBV586; 8) DYNJ41670B, UDI-DI: 10198459124228(each), 40198459124229(case) 8 1019348939164040193489391641Lot Number: 24KBA786; 9) DYNJ67227, UDI-DI: 10193489391640(each), 40193489391641(case) 9 1019532754713440195327547135Lot Number: 24KBC196; 10) DYNJ41790F, UDI-DI: 10195327547134(each), 40195327547135(case) 10 1019532767964440195327679645Lot Number: 24KBC471; 11) DYNJ49251C, UDI-DI: 10195327679644(each), 40195327679645(case) 11 1019348997408940193489974080Lot Number: 24KBG007; 12) DYNJ69733, UDI-DI: 10193489974089(each), 40193489974080(case) 12 1019348932616140193489326162Lot Number: 24KBH831; 13) DYNJ24338I, UDI-DI: 10193489326161(each), 40193489326162(case) 13 1019532725802340195327258024Lot Number: 24KBH862; 14) CDS982727L, UDI-DI: 10195327258023(each), 40195327258024(case) 14 1019845918721640198459187217Lot Number: 24KBU700; 15) DYNJ908712B, UDI-DI: 10198459187216(each), 40198459187217(case) 15 Lot 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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