Reported May 13, 2026 · Ongoing
See RES for complete list. 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?
See RES for complete list. Medline Convenience Kits
9 of 9 products
| Model / number | Product as published |
|---|---|
ACC010326 | DRAWER 6-IV FLUIDS GLOVES |
ACC010326A | DRAWER 6-IV FLUIDS GLOVES |
ACC010326B | DRAWER 6-IV FLUIDS GLOVES |
ACC010475 | DRAWER #5 |
ACC010542 | DRAWER 1 NEURO CART |
ACC010543 | DRAWER 2 NEURO CART |
ACC010722 | DRAWER 4 |
ACC010862 | SUCTION TRAY |
ACC010896 | MALIGNANT HYPERTHERMIA CART |
- Lot codes and dates
362 of 362 products
Products covered by this recall # Barcodes Product as published 1 1088994273552540889942735526Lot Number: 21CDB175; 2) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 2 1088994273552540889942735526Lot Number: 21CDB692; 3) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 3 1088994273552540889942735526Lot Number: 21LDA438; 4) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 4 1088994273552540889942735526Lot Number: 22BDB172; 5) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 5 1088994273552540889942735526Lot Number: 22HDA973; 6) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 6 1088994273552540889942735526Lot Number: 23ADA426; 7) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 7 1088994273552540889942735526Lot Number: 23BDA230; 8) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 8 1019532734714740195327347148Lot Number: 23CDC052; 9) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 9 1019532734714740195327347148Lot Number: 23CDA732; 10) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 10 1019532734714740195327347148Lot Number: 23IDB293; 11) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 11 1019532734714740195327347148Lot Number: 23LDB309; 12) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 12 1019532734714740195327347148Lot Number: 23LDB516; 13) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 13 1019532734714740195327347148Lot Number: 24ADA088; 14) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 14 1019532734714740195327347148Lot Number: 24ADA521; 15) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 15 1019532734714740195327347148Lot Number: 24ADB169; 16) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 16 1019532734714740195327347148Lot Number: 24EDB837; 17) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 17 1019532734714740195327347148Lot Number: 24GDA256; 18) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 18 1019532734714740195327347148Lot Number: 24IDA878; 19) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 19 1019532734714740195327347148Lot Number: 24JDB721; 20) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 20 1019532734714740195327347148Lot Number: 24LDA585; 21) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) - Amount recalled
- 207196 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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