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
52 of 52 products
| Model / number | Product as published |
|---|---|
DYKM2326 | OB KIT |
DYKMBNDL165 | KIT LABOR DELIVERY TUBAL LIGAT |
DYKMBNDL31 | KIT LABOR & DELIVERY D&C/D&E |
DYKMBNDL38 | KIT LABOR & DELIVERY CERCLAGE |
DYNJ0456816O | L & D PACK-LF |
DYNJ0456816P | L & D PACK-LF |
DYNJ04692S | VAGINAL DELIVERY PACK-LF |
DYNJ16621B | VAGINAL DELIVERY PACK |
DYNJ16621C | VAGINAL DELIVERY PACK |
DYNJ20546F | DELIVERY PACK-LF |
DYNJ20979I | VAGINAL DELIVERY PK |
DYNJ20979J | VAGINAL DELIVERY PK |
DYNJ24108D | VAGINAL DELIVERY PACK |
DYNJ26121I | OB PACK-LF |
DYNJ31024J | OB DELIVERY PACK |
DYNJ32139C | OB DELIVERY PACK-LF |
DYNJ33590F | DB VAG HYSTERECTOMY-LF |
DYNJ35488F | MAJOR VAGINAL PACK |
DYNJ37331C | ENS. ACCOUCHEMENT VAGINAL-LF |
DYNJ38481G | VAG DELIVERY PACK |
- Lot codes and dates
191 of 191 products
Products covered by this recall # Barcodes Product as published 1 1019348947740540193489477406Lot Number: 25KMF765; 2) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 2 1019348947740540193489477406Lot Number: 24ABK386; 3) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 3 1019348947740540193489477406Lot Number: 23KBV905; 4) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 4 1019348947740540193489477406Lot Number: 23KBA329; 5) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 5 1019348947740540193489477406Lot Number: 23HBR548; 6) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 6 1019348947740540193489477406Lot Number: 23EBP170; 7) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 7 1019348947740540193489477406Lot Number: 23BBT994; 8) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 8 1019348947740540193489477406Lot Number: 22LBB693; 9) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 9 1019348947740540193489477406Lot Number: 22KBS631; 10) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 10 1019348947740540193489477406Lot Number: 22IBB499; 11) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 11 1019348947740540193489477406Lot Number: 21LBX453; 12) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 12 1019348947740540193489477406Lot Number: 21KBM483; 13) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 13 1019348947740540193489477406Lot Number: 21JBQ910; 14) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 14 1019348947740540193489477406Lot Number: 21IBO498; 15) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 15 1019348947740540193489477406Lot Number: 21IBE978; 16) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 16 1019348947740540193489477406Lot Number: 21GBN267; 17) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 17 1019348947740540193489477406Lot Number: 21FBP760; 18) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 18 1019348947740540193489477406Lot Number: 21EBE875; 19) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 19 1019348947740540193489477406Lot Number: 21DBA335; 20) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) 20 1019348947740540193489477406Lot Number: 21ABT654; 21) DYKMBNDL165, UDI-DI: 10193489477405(each), 40193489477406(case) - Amount recalled
- 27320 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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