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
4 of 4 products
| Model / number | Product as published |
|---|---|
DYNDA2941A | CHEST TUBE INSERTION TRAY |
DYNJ83950 | CHEST/BREAST-LF |
DYNJ908337A | HERNIA REPAIR TOTE |
DYNJ908337C | HERNIA REPAIR TOTE |
- Lot codes and dates
22 of 22 products
Products covered by this recall # Barcodes Product as published 1 1019532733179540195327331796Lot Number: 23BMB940; 2) DYNDA2941A, UDI-DI: 10195327331795(each), 40195327331796(case) 2 1019532731892540195327318926Lot Number: 23FMF503; 3) DYNJ83950, UDI-DI: 10195327318925(each), 40195327318926(case) 3 1019532731892540195327318926Lot Number: 23CBG610; 4) DYNJ83950, UDI-DI: 10195327318925(each), 40195327318926(case) 4 1019532731892540195327318926Lot Number: 23FBF248; 5) DYNJ83950, UDI-DI: 10195327318925(each), 40195327318926(case) 5 1019532731892540195327318926Lot Number: 23LBR075; 6) DYNJ83950, UDI-DI: 10195327318925(each), 40195327318926(case) 6 1019532731892540195327318926Lot Number: 24CBH626; 7) DYNJ83950, UDI-DI: 10195327318925(each), 40195327318926(case) 7 1019532752481440195327524815Lot Number: 24DBT832; 8) DYNJ908337A, UDI-DI: 10195327524814(each), 40195327524815(case) 8 1019532752481440195327524815Lot Number: 23KBM234; 9) DYNJ908337A, UDI-DI: 10195327524814(each), 40195327524815(case) 9 1019532752481440195327524815Lot Number: 23KBO757; 10) DYNJ908337A, UDI-DI: 10195327524814(each), 40195327524815(case) 10 1019532752481440195327524815Lot Number: 23LBQ441; 11) DYNJ908337A, UDI-DI: 10195327524814(each), 40195327524815(case) 11 1019532752481440195327524815Lot Number: 24BBG312; 12) DYNJ908337A, UDI-DI: 10195327524814(each), 40195327524815(case) 12 1019845908592540198459085926Lot Number: 24EBM141; 13) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 13 1019845908592540198459085926Lot Number: 24HBW695; 14) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 14 1019845908592540198459085926Lot Number: 24IBN719; 15) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 15 1019845908592540198459085926Lot Number: 24KBK455; 16) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 16 1019845908592540198459085926Lot Number: 25ABG235; 17) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 17 1019845908592540198459085926Lot Number: 25BBO546; 18) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 18 1019845908592540198459085926Lot Number: 25DBG687; 19) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 19 1019845908592540198459085926Lot Number: 25DBQ261; 20) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) 20 1019845908592540198459085926Lot Number: 25FBF535; 21) DYNJ908337C, UDI-DI: 10198459085925(each), 40198459085926(case) - Amount recalled
- 892 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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