MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF recall (Medline Industries, LP)
Medical deviceClass IIOngoing
Summary: Medline Industries, LP is recalling 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.
What is being recalled
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.
Why
Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE. (states named: California)
How to tell if yours is affected
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.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-0276-2027 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | September 9, 2026 |
| Reported | October 28, 2026 |
| Company | Medline Industries, LP |
| Company location | Northfield, IL, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 2229 kits |
More recalls from Medline Industries, LP · all medical device recalls · recalls from September 2026