Medline Industries, LP recalls MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF
- Recalling company
- Medline Industries, LP
- Product
- MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF, Medline Kit Number/SKU DYNJ16127N; 2) NYGH-DELIVERY PACK-LF, Medline Kit Number/SKU DYNJ27206D; 3) OB/GYN, Medline Kit Number/SKU DYNJ911652.
- 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
- 2229 kits
- Lot / codes
- Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26FBB857; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26EBA908; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26CBV797; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 26ABM708; Medline Kit Number/SKU DYNJ16127N, UDI/DI 10198459449826 (each) 40198459449827 (case), Lot Number 25KBQ582; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26GBV395; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26FBO061; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26DBF331; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 26BBT983; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 25LBJ546; Medline Kit Number/SKU DYNJ27206D, UDI/DI 10198459353611 (each) 40198459353612 (case), Lot Number 25KBK623; Medline Kit Number/SKU DYNJ911652, UDI/DI 10198459481673 (each) 40198459481674 (case), Lot Number 26DME349.
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0276-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0276-2027 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.