CLASS II · ModerateFDA

Medline Industries, LP recalls MEDLINE medical convenience kits labeled as

📅 Sep 9, 2026 · 📍 Nationwide

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: 26965 kits
Lot / codes: Medline Kit Number/SKU CDS980963D, UDI/DI 10889942942091 (each) 40889942942092 (case), Lot Number 26HBU410; Medline Kit Number/SKU CDS980963D, UDI/DI 10889942942091 (each) 40889942942092 (case), Lot Number 26GBU519; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26EBR697; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26DBS199; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26CBO921; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 26CBF309; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 25LBJ133; Medline Kit Number/SKU CDS983917O, UDI/DI 10195327583392 (each) 40195327583393 (case), Lot Number 25KBK360; Medline Kit Number/SKU CDS984264J, UDI/DI 10198459303142 (each) 40198459303143 (case), Lot Number 26FBM729; Medline Kit Number/SKU CDS984264J, UDI/DI 10198459303142 (each) 40198459303143 (case), Lot Number 25KBA584; Medline Kit Number/SKU DYNJT0473L, UDI/DI 10198459727924 (each) 40198459727925 (case), Lot Number 26EMH174; Medline Kit Number/SKU DYNJT10306, UDI/DI 10198459787232 (each) 40198459787233 (case), Lot Number 26FBD165; Medline Kit Number/SKU DYNJT2552G, UDI/DI 10198459334733 (each) 40198459334734 (case), Lot Number 26HMB198; Medline Kit Number/SKU DYNJT2552G, UDI/DI 10198459334733 (each) 40198459334734 (cas
Company location: Northfield, IL
Recall type: Voluntary: Firm initiated
Recall number: Z-0275-2027
Agency: U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0275-2027 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.