Z-0751-2023 Class II Terminated
FDA device recall Z-0751-2023 was initiated by Medical Action Industries, Inc. 306 on November 4, 2022 and is designated Class II. Reason for recall: XXX The recall status is terminated (terminated March 18, 2026). Affected quantity: 198 cases.
Recall Details
- Product Type
- Devices
- Report Date
- December 28, 2022
- Initiation Date
- November 4, 2022
- Termination Date
- March 18, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 198 cases
Product Description
Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
Reason for Recall
XXX
Distribution Pattern
US Nationwide distribution in the state of VA.
Code Information
UDI/DI 10809160156681, Lot Numbers: 297223, 297418