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
48 of 48 products
| Model / number | Product as published |
|---|---|
CDS985094F | OR ARTERIOGRAM |
DYKMBNDL153 | KIT SURG ONC LAP DIAG/CV CATH |
DYKMBNDL4A | KIT ACES INSERT PERCUTANEOUS T |
DYKMBNDL4B | KIT ACES INSERT PERCUTANEOUS T |
DYNDA2076C | VEIN PROCEDURE KIT |
DYNJ0150605AC | CARDIAC CATH PACK-LF |
DYNJ0648473Y | CATH LAB PACK-LF |
DYNJ0803367I | NBMC CATH PACK-LF |
DYNJ0954970I | ANGIO PACK-LF |
DYNJ19946M | CARDIAC CATH PACK |
DYNJ30955I | CATH LAB PACK |
DYNJ31773K | CATH LAB PACK |
DYNJ33061D | CATH PACK-LF |
DYNJ33620D | DB CCL OAKWOOD PACK-LF |
DYNJ35300M | CARDIAC CATH PACK MRH-LF |
DYNJ35643C | CATH LAB PK |
DYNJ39066B | CARDIAC CATH PACK-LF |
DYNJ43101C | CATH PACK-LF |
DYNJ43415D | OR ANGIO PACK-LF |
DYNJ43415F | OR ANGIO PACK-LF |
- Lot codes and dates
170 of 170 products
Products covered by this recall # Barcodes Product as published 1 1019348947844040193489478441Lot Number: 25AMG933; 2) DYKMBNDL153, UDI-DI: 10193489478440(each), 40193489478441(case) 2 1019348947844040193489478441Lot Number: 22ABO093; 3) DYKMBNDL153, UDI-DI: 10193489478440(each), 40193489478441(case) 3 1019348947844040193489478441Lot Number: 21LBJ748; 4) DYKMBNDL153, UDI-DI: 10193489478440(each), 40193489478441(case) 4 1019348947844040193489478441Lot Number: 21BBG516; 5) DYKMBNDL153, UDI-DI: 10193489478440(each), 40193489478441(case) 5 1019348990451240193489904513Lot Number: 21ABI976; 6) DYKMBNDL4A, UDI-DI: 10193489904512(each), 40193489904513(case) 6 1019348990451240193489904513Lot Number: 22ALA279; 7) DYKMBNDL4A, UDI-DI: 10193489904512(each), 40193489904513(case) 7 1019348990451240193489904513Lot Number: 21KLA100; 8) DYKMBNDL4A, UDI-DI: 10193489904512(each), 40193489904513(case) 8 1019532720058940195327200580Lot Number: 21GLA930; 9) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 9 1019532720058940195327200580Lot Number: 25ALA014; 10) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 10 1019532720058940195327200580Lot Number: 24FLA816; 11) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 11 1019532720058940195327200580Lot Number: 24CLA777; 12) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 12 1019532720058940195327200580Lot Number: 23KLA402; 13) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 13 1019532720058940195327200580Lot Number: 23JLA979; 14) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 14 1019532720058940195327200580Lot Number: 23ILA268; 15) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 15 1019532720058940195327200580Lot Number: 23HLA316; 16) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 16 1019532720058940195327200580Lot Number: 23GLA710; 17) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 17 1019532720058940195327200580Lot Number: 23GLA176; 18) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 18 1019532720058940195327200580Lot Number: 23BLA583; 19) DYKMBNDL4B, UDI-DI: 10195327200589(each), 40195327200580(case) 19 1019845900120840198459001209Lot Number: 22HLB260; 20) DYNDA2076C, UDI-DI: 10198459001208(each), 40198459001209(case) 20 1019845900120840198459001209Lot Number: 24LMB205; 21) DYNDA2076C, UDI-DI: 10198459001208(each), 40198459001209(case) - Amount recalled
- 30958 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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