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
Is this the product you have?
Medline Convenience Kits
58 of 58 products
| Model / number | Product as published |
|---|---|
ACC010499 | PLASTIC BIN W/MISC KITS |
DYKMBNDL117C | KIT UROLOGY URETHROPLASTY |
DYKMBNDL158 | KIT PLASTIC INSERT TISSUE EXPA |
DYKMBNDL170 | KIT PLASTIC ABDOMINOPLASTY |
DYKMBNDL170A | KIT PLASTIC ABDOMINOPLASTY |
DYKMBNDL170B | KIT PLASTIC ABDOMINOPLASTY |
DYKMBNDL182 | KIT PLASTIC ABDOMINOPLASTY |
DYKMBNDL182A | KIT PLASTIC ABDOMINOPLASTY |
DYKMBNDL182B | KIT PLASTIC ABDOMINOPLASTY |
DYKMBNDL183 | KIT PLASTIC ROTATIONAL FLAP |
DYKMBNDL183A | KIT PLASTIC ROTATIONAL FLAP |
DYKMBNDL183B | KIT PLASTIC ROTATIONAL FLAP |
DYKMBNDL34A | KIT STC FACIAL FRACTURE |
DYKMBNDL39 | KIT SURG ONC MASTECTOMY A |
DYKMBNDL39A | KIT SURG ONC MASTECTOMY A |
DYKMBNDL39C | KIT SURG ONC MASTECTOMY |
DYKMBNDL46 | KIT PLASTICS BREAST REDUCTION |
DYKMBNDL54 | KIT STC PLASTIC FREE FLAP |
DYKMBNDL69 | KIT PLASTICS BREAST REDUCTION |
DYKMBNDL69A | KIT PLASTICS BREAST REDUCTION |
- Lot codes and dates
251 of 251 products
Products covered by this recall # Barcodes Product as published 1 1019348984570940193489845700Lot Number: 25BDB702; 2) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 2 1019348984570940193489845700Lot Number: 25BDA228; 3) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 3 1019348984570940193489845700Lot Number: 25ADB705; 4) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 4 1019348984570940193489845700Lot Number: 24JDA650; 5) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 5 1019348984570940193489845700Lot Number: 24IDA403; 6) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 6 1019348984570940193489845700Lot Number: 23LDC086; 7) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 7 1019348984570940193489845700Lot Number: 23IDB182; 8) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 8 1019348984570940193489845700Lot Number: 23HDB786; 9) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 9 1019348984570940193489845700Lot Number: 21JDB530; 10) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 10 1019348984570940193489845700Lot Number: 21HDB434; 11) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 11 1019348984570940193489845700Lot Number: 21GDB740; 12) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 12 1019348984570940193489845700Lot Number: 21FDA888; 13) ACC010499, UDI-DI: 10193489845709(each), 40193489845700(case) 13 1019532737110440195327371105Lot Number: 21DDA661; 14) DYKMBNDL117C, UDI-DI: 10195327371104(each), 40195327371105(case) 14 1019348947826640193489478267Lot Number: 23DLA834; 15) DYKMBNDL158, UDI-DI: 10193489478266(each), 40193489478267(case) 15 1019348947826640193489478267Lot Number: 21CBE548; 16) DYKMBNDL158, UDI-DI: 10193489478266(each), 40193489478267(case) 16 1019348947745040193489477451Lot Number: 21ABI978; 17) DYKMBNDL170, UDI-DI: 10193489477450(each), 40193489477451(case) 17 1019348947745040193489477451Lot Number: 22IBC515; 18) DYKMBNDL170, UDI-DI: 10193489477450(each), 40193489477451(case) 18 1019348947745040193489477451Lot Number: 22HBN456; 19) DYKMBNDL170, UDI-DI: 10193489477450(each), 40193489477451(case) 19 1019348947745040193489477451Lot Number: 22EBA143; 20) DYKMBNDL170, UDI-DI: 10193489477450(each), 40193489477451(case) 20 1019348947745040193489477451Lot Number: 21IBV640; 21) DYKMBNDL170, UDI-DI: 10193489477450(each), 40193489477451(case) - Amount recalled
- 4757 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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