FDA Device recall Z-1947-2021
novaplus, General Purpose Kit, Cat
- FDA Device
- Class II
- terminated
- Published 2021-06-30
On 2021-06-30 the FDA classified a Class II recall of novaplus, General Purpose Kit, Cat by Medical Action Industries 306, citing there is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1947-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-05-11 |
| Published | 2021-06-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medical Action Industries 306 |
| Distribution | US |
Product
novaplus, General Purpose Kit, Cat. No. 56603
Reason
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Identifiers
| code_info | Batch Numbers: 0000275724, Exp. 02/15/2022; 0000277619, Exp. 04/15/2022 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1947-2021%22
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