Z-1394-2024 Class II Ongoing
FDA device recall Z-1394-2024 was initiated by Medical Action Industries, Inc. 306 on January 15, 2024 and is designated Class II. Reason for recall: The kits contain saline flush syringes which were recalled by the supplier. The recall status is ongoing. Affected quantity: 206,200 kits.
Recall Details
- Product Type
- Devices
- Report Date
- April 3, 2024
- Initiation Date
- January 15, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 206,200 kits
Product Description
IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Reason for Recall
The kits contain saline flush syringes which were recalled by the supplier.
Distribution Pattern
US Nationwide distribution in the states of MN and ND. There as no foreign/military/government distribution.
Code Information
Lot numbers 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311741, 312807, and 313961;UDI-DI 10809160020388.