Z-2007-2026 Class I Ongoing
FDA device recall Z-2007-2026 was initiated by Medical Action Industries, Inc. 306 on March 17, 2026 and is designated Class I. Reason for recall: Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold" The recall status is ongoing. Affected quantity: 2030 kits.
Recall Details
- Product Type
- Devices
- Report Date
- May 13, 2026
- Initiation Date
- March 17, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2030 kits
Product Description
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Reason for Recall
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
Distribution Pattern
US distribution to state of: AZ OUS: None
Code Information
UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789