Reported Feb 25, 2026 · Ongoing
Medline Convenience Kits
Medline Industries, LP
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 · 3 Lakes Dr · Northfield, IL · 60093-2753
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Medline Convenience Kits
10 of 10 products
| Model / number | Product as published |
|---|---|
DYKE1743 | ENDO KIT W/SYRINGE |
DYNJ0800934D | BGMC ANGIOGRAPHY PACK-LF |
DYNJ0842873J | GENERAL ENDO PACK-LF |
DYNJ43415C | OR ANGIO PACK-LF |
DYNJ44066A | ANGIO PACK II |
DYNJ61978A | SOUTH CATH LAB PACK |
DYNJ63542B | BIOPSY ANGIO TRAY ALEX |
DYNJ907452 | SURGICAL TECH KIT |
DYNJC2371G | ANGIOGRAPHY PACK |
PHS853965G | SPECTRUM HEALTH CATH PACK-LF |
- Lot codes and dates
20 of 20 products
Products covered by this recall # Barcodes Product as published 1 1019348929460640193489294607Lot Number: 23KBQ544; 2) DYKE1743, UDI-DI: 10193489294606(each), 40193489294607(case) 2 1019348939888540193489398886Lot Number: 23JBO193; 3) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 3 1019348939888540193489398886Lot Number: 21EBQ851; 4) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 4 1019348939888540193489398886Lot Number: 21DBA951; 5) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 5 1019348939888540193489398886Lot Number: 21BKA527; 6) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 6 1019348944891740193489448918Lot Number: 21AKB217; 7) DYNJ0842873J, UDI-DI: 10193489448917(each), 40193489448918(case) 7 1019348990139940193489901390Lot Number: 21ADA204; 8) DYNJ43415C, UDI-DI: 10193489901399(each), 40193489901390(case) 8 1019348990139940193489901390Lot Number: 22EBI127; 9) DYNJ43415C, UDI-DI: 10193489901399(each), 40193489901390(case) 9 1019348990139940193489901390Lot Number: 22EBF322; 10) DYNJ43415C, UDI-DI: 10193489901399(each), 40193489901390(case) 10 1088827753802340888277538024Lot Number: 22CBF108; 11) DYNJ44066A, UDI-DI: 10888277538023(each), 40888277538024(case) 11 1088827753802340888277538024Lot Number: 22CLA012; 12) DYNJ44066A, UDI-DI: 10888277538023(each), 40888277538024(case) 12 1088827753802340888277538024Lot Number: 22BLA508; 13) DYNJ44066A, UDI-DI: 10888277538023(each), 40888277538024(case) 13 1088827753802340888277538024Lot Number: 21KLA332; 14) DYNJ44066A, UDI-DI: 10888277538023(each), 40888277538024(case) 14 1088827753802340888277538024Lot Number: 21HLA812; 15) DYNJ44066A, UDI-DI: 10888277538023(each), 40888277538024(case) 15 1019348972930640193489729307Lot Number: 21CLA325; 16) DYNJ61978A, UDI-DI: 10193489729306(each), 40193489729307(case) 16 1019348939863240193489398633Lot Number: 20LDB953; 17) DYNJ63542B, UDI-DI: 10193489398632(each), 40193489398633(case) 17 1019348942288740193489422888Lot Number: 23DBP359; 18) DYNJ907452, UDI-DI: 10193489422887(each), 40193489422888(case) 18 1088994249467540889942494676Lot Number: 20LBW791; 19) DYNJC2371G, UDI-DI: 10889942494675(each), 40889942494676(case) 19 1019348924946040193489249461Lot Number: 23BBT999; 20) PHS853965G, UDI-DI: 10193489249460(each), 40193489249461(case) 20 Lot Number: 21ADA067 - Amount recalled
- 3561 units
This recall covers 43 products
The agency filed one notice per product. You are reading one of them; the other 42 are below.
30 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
This product could cause temporary or reversible health problems — stop using it.
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