Reported May 13, 2026 · Ongoing
Medline Surgical Drapes
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 Surgical Drapes
54 of 54 products
| Model / number | Product as published |
|---|---|
DYNJP2410 | SHEET,DRAPE,40X58,STERILE |
DYNJP2411 | DRAPE,SHEET,ECONOMY,40X58",ST,20/CS |
DYNJP2412 | SHEET,DRAPE, 40X70,STERILE |
DYNJP2412T | DRAPE,MEDIUM,TAPE,40X70",ST,50/CS |
DYNJP2414 | SHEET,DRAPE,53X77,STERILE |
DYNJP2414R | DRAPE,SHEET,3/4,53X77",ST,20/CS |
DYNJP2414UG | DRAPE,SHEET,ULTRAGARD,20/CS |
DYNJP2416 | DRAPE,RNF,53X77",ST,20/CS |
DYNJP2417 | SHEET,DRAPE,70X85,STERILE |
DYNJP2418 | DRAPE,FILM SHEET,44X65",ST,20/CS |
DYNJP2419 | DRAPE,SHEET,70X100",ST,12/CS |
DYNJP2462 | LEGGINGS,33X49",XL,PAIR,ST,CLR,20/CS |
DYNJP2491 | DRAPE,CHEST,FENESTRATION,15X10",ST,12/CS |
DYNJP2492 | DRAPE,MINOR PROC,6X6" FEN, ST,10/CS |
DYNJP2498 | SHEET, DRAPE, SPLIT, ST,10/CS |
DYNJP3003 | DRAPE,LAPAROTOMY,T-SHEET,ST,12/CS |
DYNJP3003UG | DRAPE,LAPAROTOMY,T,ULTRAGARD,12/CS |
DYNJP3008 | DRAPE,LAPAROTOMY,POUCH,ST,12/CS |
DYNJP3008UG | DRAPE,LAPAROTOMY,POUCH ULTRAGARD,12/CS |
DYNJP3009 | DRAPE,LAPAROTOMY,T,PEDIATRIC,ST,10/CS |
- Lot codes and dates
350 of 350 products
Products covered by this recall # Barcodes Product as published 1 1008019673969140080196739692Lot Number: 30525050127; 2) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 2 1008019673969140080196739692Lot Number: 30525070161; 3) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 3 1008019673969140080196739692Lot Number: 30525070250; 4) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 4 1008019673969140080196739692Lot Number: 30525060147; 5) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 5 1008019673969140080196739692Lot Number: 30522030151; 6) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 6 1008019673969140080196739692Lot Number: 30522070033; 7) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 7 1008019673969140080196739692Lot Number: 30522080015; 8) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 8 1008019673969140080196739692Lot Number: 30522080067; 9) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 9 1008019673969140080196739692Lot Number: 30522090028; 10) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 10 1008019673969140080196739692Lot Number: 30522100060; 11) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 11 1008019673969140080196739692Lot Number: 30522100091; 12) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 12 1008019673969140080196739692Lot Number: 30522120121; 13) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 13 1008019673969140080196739692Lot Number: 30522120207; 14) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case) 14 1008019674548740080196745488Lot Number: 30523010081; 15) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case) 15 1008019674548740080196745488Lot Number: 30525030122; 16) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case) 16 1008019674548740080196745488Lot Number: 30525050190; 17) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case) 17 1008019674548740080196745488Lot Number: 30525040163; 18) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case) 18 1008019674548740080196745488Lot Number: 30525060157; 19) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case) 19 1008019674548740080196745488Lot Number: 30525080250; 20) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case) 20 1008019674548740080196745488Lot Number: 30523010024; 21) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case) - Amount recalled
- 14927765 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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