Z-1331-2026 Class II Ongoing
FDA device recall Z-1331-2026 was initiated by Medline Industries, LP on December 24, 2025 and is designated Class II. Reason for recall: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the a… The recall status is ongoing. Affected quantity: 7380 kits.
Recall Details
- Product Type
- Devices
- Report Date
- February 18, 2026
- Initiation Date
- December 24, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7380 kits
Product Description
Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU RWM-DC57KC.
Reason for Recall
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Distribution Pattern
US Nationwide distribution.
Code Information
1) Kit SKU DYNDH1576, UDI/DI 10193489437041, Lot Number 25EBP737; 2) Kit SKU RWM-DC57KC, UDI/DI 10889942582013, Lot Number 25EBE082.