Z-1335-2026 Class II Ongoing
FDA device recall Z-1335-2026 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: 216 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
- 216 kits
Product Description
Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A
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
UDI/DI 10195327379292, Lot Number 25EBJ785