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
67 of 67 products
| Model / number | Product as published |
|---|---|
ACC010326 | DRAWER 6-IV FLUIDS GLOVES |
ACC010326A | DRAWER 6-IV FLUIDS GLOVES |
ACC010475 | DRAWER #5 |
ACC010542 | DRAWER 1 NEURO CART |
ACC010543 | DRAWER 2 NEURO CART |
ACC010722 | DRAWER 4 |
ACC010896 | MALIGNANT HYPERTHERMIA CART |
CDS860063U | LIVER TRANSPLANT #57 CDS-2 |
CDS860066T | THOROCOTOMY CDS #24-RF |
CDS981795G | CYSTO |
CDS982414N | MAJOR PROCEDURE CDS |
CDS982823R | TOTAL KNEE CDS |
CDS982895I | VASCULAR CDS-1 |
CDS983069F | CHP COCHLEAR SUPPLEMENT CDS |
CDS983376S | HEART CABG CDS |
CDS983611N | CRANIOTOMY |
CDS983653K | CUH KIDNEY TRANSPLANT CDS |
CDS983653L | CUH KIDNEY TRANSPLANT CDS |
CDS983653M | CUH KIDNEY TRANSPLANT CDS |
CDS983908Q | MAJOR ABDOMINAL CDS |
- Lot codes and dates
360 of 360 products
Products covered by this recall # Barcodes Product as published 1 1088994273552540889942735526Lot Number: 22HDA973; 2) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 2 1088994273552540889942735526Lot Number: 22BDB172; 3) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 3 1088994273552540889942735526Lot Number: 21LDA438; 4) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 4 1088994273552540889942735526Lot Number: 21CDB692; 5) ACC010326, UDI-DI: 10889942735525(each), 40889942735526(case) 5 1019532734714740195327347148Lot Number: 21CDB175; 6) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 6 1019532734714740195327347148Lot Number: 24GDA256; 7) ACC010326A, UDI-DI: 10195327347147(each), 40195327347148(case) 7 1019348946901140193489469012Lot Number: 23IDB293; 8) ACC010475, UDI-DI: 10193489469011(each), 40193489469012(case) 8 1019348946901140193489469012Lot Number: 23EDC028; 9) ACC010475, UDI-DI: 10193489469011(each), 40193489469012(case) 9 1019348946901140193489469012Lot Number: 23EDB192; 10) ACC010475, UDI-DI: 10193489469011(each), 40193489469012(case) 10 1019348946901140193489469012Lot Number: 23EDA657; 11) ACC010475, UDI-DI: 10193489469011(each), 40193489469012(case) 11 1019348946901140193489469012Lot Number: 22LDA361; 12) ACC010475, UDI-DI: 10193489469011(each), 40193489469012(case) 12 1019348946901140193489469012Lot Number: 22KDB086; 13) ACC010475, UDI-DI: 10193489469011(each), 40193489469012(case) 13 1019348946901140193489469012Lot Number: 22JDB707; 14) ACC010475, UDI-DI: 10193489469011(each), 40193489469012(case) 14 1019348999727940193489997270Lot Number: 21BDA319; 15) ACC010542, UDI-DI: 10193489997279(each), 40193489997270(case) 15 1019348999727940193489997270Lot Number: 24DDA266; 16) ACC010542, UDI-DI: 10193489997279(each), 40193489997270(case) 16 1019348999727940193489997270Lot Number: 23JDA838; 17) ACC010542, UDI-DI: 10193489997279(each), 40193489997270(case) 17 1019348999727940193489997270Lot Number: 22FDB178; 18) ACC010542, UDI-DI: 10193489997279(each), 40193489997270(case) 18 1019348999727940193489997270Lot Number: 22DDB648; 19) ACC010542, UDI-DI: 10193489997279(each), 40193489997270(case) 19 1019348999728640193489997287Lot Number: 21KDA051; 20) ACC010543, UDI-DI: 10193489997286(each), 40193489997287(case) 20 1019348999728640193489997287Lot Number: 25KDB023; 21) ACC010543, UDI-DI: 10193489997286(each), 40193489997287(case) - Amount recalled
- 154427 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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