Medline Industries, LP recalls MEDLINE medical convenience kits labeled as:
- Recalling company
- Medline Industries, LP
- Product
- MEDLINE medical convenience kits labeled as: (list truncated)
- Reason
- Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Sep 9, 2026
- Reported
- Oct 28, 2026
- Distribution
- Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.
- Status
- Ongoing
- Quantity
- 146971 kits
- Lot / codes
- Medline Kit Number/SKU DYNJ40917B, UDI/DI 10195327599928 (each) 40195327599929 (case), Lot number 26HBB007; Medline Kit Number/SKU DYNJ905792F, UDI/DI 10198459411625 (each) 40198459411626 (case), Lot number 26FMH990; Medline Kit Number/SKU CDSCCR611R, UDI/DI 10198459001376 (each) 40198459001377 (case), Lot number 25KBM623; Medline Kit Number/SKU CDSCCR611S, UDI/DI 10198459610233 (each) 40198459610234 (case), Lot number 26HBE979; Medline Kit Number/SKU CDSCCR611S, UDI/DI 10198459610233 (each) 40198459610234 (case), Lot number 26GBK211; Medline Kit Number/SKU CDSCCR611S, UDI/DI 10198459610233 (each) 40198459610234 (case), Lot number 26EBK060; Medline Kit Number/SKU CDSCCR611S, UDI/DI 10198459610233 (each) 40198459610234 (case), Lot number 26ABQ736; Medline Kit Number/SKU CDSCCR611S, UDI/DI 10198459610233 (each) 40198459610234 (case), Lot number 26ABF499; Medline Kit Number/SKU CDS820031J, UDI/DI 10193489642971 (each) 40193489642972 (case), Lot number 26CMG521; Medline Kit Number/SKU CDS820031J, UDI/DI 10193489642971 (each) 40193489642972 (case), Lot number 25KBD161; Medline Kit Number/SKU CDS820075X, UDI/DI 10198459311550 (each) 40198459311551 (case), Lot number 26HMK631; Medline Kit Number/SKU CDS820075X, UDI/DI 10198459311550 (each) 40198459311551 (case), Lot number 26HME176; Medline Kit Number/SKU CDS820075X, UDI/DI 10198459311550 (each) 40198459311551 (case), Lot number 26DMH183; Medline Kit Number/SKU CDS820075X, UDI/DI 10198459311550 (each) 40198459311551 (ca
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0278-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0278-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.