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
35 of 35 products
| Model / number | Product as published |
|---|---|
DYKMBNDL104 | KIT OPHTHALMIC RUPTURE GLOBE |
DYKMBNDL104A | KIT OPHTHALMIC RUPTURE GLOBE |
DYKMBNDL159 | KIT OPHTHALMOLOGY CORNEAL TRAN |
DYKMBNDL180 | KIT OPHTHALMOLOGY CATARACT |
DYKMBNDL42 | KIT OPHTHALMOLOGY EYE MUSCLE |
DYKMBNDL43B | KIT SURG ONC PORT INSERTION |
DYKMBNDL84B | KIT SURG ONC EXCISION BREAST |
DYKMBNDL98 | KIT OPTHAMOLOGY BASIC |
DYKMBNDL98A | KIT OPTHAMOLOGY BASIC |
DYKMBNDL98B | KIT OPTHAMOLOGY BASIC |
DYNJ17219C | MINOR EYE PACK |
DYNJ38791M | PEDS EYE/MUSCLE PACK |
DYNJ41207C | EYE PACK |
DYNJ42043I | OPHTHALMIC PACK |
DYNJ44852J | BREAST RECONSTRUCTION-HOULE |
DYNJ45585C | CUSTOM EYE PACK HA-LF |
DYNJ47859B | EYE PLASTIC PACK |
DYNJ47859C | EYE PLASTIC PACK |
DYNJ53019A | CATARACT PACK |
DYNJ54869A | CATARACT PACK |
- Lot codes and dates
113 of 113 products
Products covered by this recall # Barcodes Product as published 1 1019348947894540193489478946Lot Number: 22GBP895; 2) DYKMBNDL104, UDI-DI: 10193489478945(each), 40193489478946(case) 2 1019348947894540193489478946Lot Number: 21IBV636; 3) DYKMBNDL104, UDI-DI: 10193489478945(each), 40193489478946(case) 3 1019348947894540193489478946Lot Number: 21FBP706; 4) DYKMBNDL104, UDI-DI: 10193489478945(each), 40193489478946(case) 4 1019532724062240195327240623Lot Number: 21ABV400; 5) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case) 5 1019532724062240195327240623Lot Number: 24EBU650; 6) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case) 6 1019532724062240195327240623Lot Number: 23HBV380; 7) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case) 7 1019532724062240195327240623Lot Number: 22KBO773; 8) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case) 8 1019532724062240195327240623Lot Number: 22JBS907; 9) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case) 9 1019532724062240195327240623Lot Number: 22JBS899; 10) DYKMBNDL104A, UDI-DI: 10195327240622(each), 40195327240623(case) 10 1019348947827340193489478274Lot Number: 22HBX475; 11) DYKMBNDL159, UDI-DI: 10193489478273(each), 40193489478274(case) 11 1019348947846440193489478465Lot Number: 21ABQ655; 12) DYKMBNDL180, UDI-DI: 10193489478464(each), 40193489478465(case) 12 1019348947846440193489478465Lot Number: 21FBP773; 13) DYKMBNDL180, UDI-DI: 10193489478464(each), 40193489478465(case) 13 1019348947846440193489478465Lot Number: 21BBM375; 14) DYKMBNDL180, UDI-DI: 10193489478464(each), 40193489478465(case) 14 1019348947888440193489478885Lot Number: 21ABT655; 15) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case) 15 1019348947888440193489478885Lot Number: 21KLA277; 16) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case) 16 1019348947888440193489478885Lot Number: 21ILA655; 17) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case) 17 1019348947888440193489478885Lot Number: 21HLA179; 18) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case) 18 1019348947888440193489478885Lot Number: 21FLA394; 19) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case) 19 1019348947888440193489478885Lot Number: 21BBK655; 20) DYKMBNDL42, UDI-DI: 10193489478884(each), 40193489478885(case) 20 1019532736920040195327369201Lot Number: 21ABR620; 21) DYKMBNDL43B, UDI-DI: 10195327369200(each), 40195327369201(case) - Amount recalled
- 4853 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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