Reported Feb 25, 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

Products covered by this recall
Model / numberProduct as published
DYNJP2410SHEET,DRAPE,40X58,STERILE
DYNJP2411DRAPE,SHEET,ECONOMY,40X58",ST,20/CS
DYNJP2412SHEET,DRAPE, 40X70,STERILE
DYNJP2412TDRAPE,MEDIUM,TAPE,40X70",ST,50/CS
DYNJP2414SHEET,DRAPE,53X77,STERILE
DYNJP2414RDRAPE,SHEET,3/4,53X77",ST,20/CS
DYNJP2414UGDRAPE,SHEET,ULTRAGARD,20/CS
DYNJP2416DRAPE,RNF,53X77",ST,20/CS
DYNJP2417SHEET,DRAPE,70X85,STERILE
DYNJP2418DRAPE,FILM SHEET,44X65",ST,20/CS
DYNJP2419DRAPE,SHEET,70X100",ST,12/CS
DYNJP2462LEGGINGS,33X49",XL,PAIR,ST,CLR,20/CS
DYNJP2491DRAPE,CHEST,FENESTRATION,15X10",ST,12/CS
DYNJP2492DRAPE,MINOR PROC,6X6" FEN, ST,10/CS
DYNJP2498SHEET, DRAPE, SPLIT, ST,10/CS
DYNJP3003DRAPE,LAPAROTOMY,T-SHEET,ST,12/CS
DYNJP3003UGDRAPE,LAPAROTOMY,T,ULTRAGARD,12/CS
DYNJP3008DRAPE,LAPAROTOMY,POUCH,ST,12/CS
DYNJP3008UGDRAPE,LAPAROTOMY,POUCH ULTRAGARD,12/CS
DYNJP3009DRAPE,LAPAROTOMY,T,PEDIATRIC,ST,10/CS
Lot codes and dates

350 of 350 products

Products covered by this recall
#BarcodesProduct as published
11008019673969140080196739692Lot Number: 30525050127; 2) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
21008019673969140080196739692Lot Number: 30525070161; 3) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
31008019673969140080196739692Lot Number: 30525070250; 4) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
41008019673969140080196739692Lot Number: 30525060147; 5) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
51008019673969140080196739692Lot Number: 30522030151; 6) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
61008019673969140080196739692Lot Number: 30522070033; 7) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
71008019673969140080196739692Lot Number: 30522080015; 8) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
81008019673969140080196739692Lot Number: 30522080067; 9) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
91008019673969140080196739692Lot Number: 30522090028; 10) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
101008019673969140080196739692Lot Number: 30522100060; 11) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
111008019673969140080196739692Lot Number: 30522100091; 12) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
121008019673969140080196739692Lot Number: 30522120121; 13) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
131008019673969140080196739692Lot Number: 30522120207; 14) DYNJP2410, UDI-DI: 10080196739691(each), 40080196739692(case)
141008019674548740080196745488Lot Number: 30523010081; 15) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case)
151008019674548740080196745488Lot Number: 30525030122; 16) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case)
161008019674548740080196745488Lot Number: 30525050190; 17) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case)
171008019674548740080196745488Lot Number: 30525040163; 18) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case)
181008019674548740080196745488Lot Number: 30525060157; 19) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case)
191008019674548740080196745488Lot Number: 30525080250; 20) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case)
201008019674548740080196745488Lot Number: 30523010024; 21) DYNJP2411, UDI-DI: 10080196745487(each), 40080196745488(case)
Amount recalled
14,927,765 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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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, 6:20 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.