Reported May 13, 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
Is this the product you have?
Medline Convenience Kits
12 of 12 products
| Model / number | Product as published |
|---|---|
00-401824AA | ANGIO PROCEDURE PACK |
DYKE1743 | ENDO KIT W/SYRINGE |
DYNJ0800934D | BGMC ANGIOGRAPHY PACK-LF |
DYNJ0842873J | GENERAL ENDO PACK-LF |
DYNJ32328 | ANGIO PROCEDURE PACK |
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
36 of 36 products
Products covered by this recall # Barcodes Product as published 1 1019348945588540193489455886Lot Number: 23ABN008; 2) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 2 1019348945588540193489455886Lot Number: 23CBM469; 3) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 3 1019348945588540193489455886Lot Number: 23EBH500; 4) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 4 1019348945588540193489455886Lot Number: 23GBE369; 5) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 5 1019348945588540193489455886Lot Number: 23IBE051; 6) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 6 1019348945588540193489455886Lot Number: 23IBU695; 7) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 7 1019348945588540193489455886Lot Number: 23KBD600; 8) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 8 1019348945588540193489455886Lot Number: 23LBC152; 9) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 9 1019348945588540193489455886Lot Number: 24ABR800; 10) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 10 1019348945588540193489455886Lot Number: 24CBC183; 11) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 11 1019348945588540193489455886Lot Number: 24DBS738; 12) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 12 1019348945588540193489455886Lot Number: 24FBN230; 13) 00-401824AA, UDI-DI: 10193489455885(each), 40193489455886(case) 13 1019348929460640193489294607Lot Number: 24HBB532; 14) DYKE1743, UDI-DI: 10193489294606(each), 40193489294607(case) 14 1019348929460640193489294607Lot Number: 23JBO193; 15) DYKE1743, UDI-DI: 10193489294606(each), 40193489294607(case) 15 1019348929460640193489294607Lot Number: 23KBQ544; 16) DYKE1743, UDI-DI: 10193489294606(each), 40193489294607(case) 16 1019348939888540193489398886Lot Number: 23LBJ521; 17) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 17 1019348939888540193489398886Lot Number: 21AKB217; 18) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 18 1019348939888540193489398886Lot Number: 21BKA527; 19) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 19 1019348939888540193489398886Lot Number: 21DBA951; 20) DYNJ0800934D, UDI-DI: 10193489398885(each), 40193489398886(case) 20 1019348944891740193489448918Lot Number: 21EBQ851; 21) DYNJ0842873J, UDI-DI: 10193489448917(each), 40193489448918(case) - Amount recalled
- 6961 units
This recall covers 42 products
The agency filed one notice per product. You are reading one of them; the other 41 are below.
29 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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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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