FDA Device recall Z-1554-2022
NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"
- FDA Device
- Class II
- ongoing
- Published 2022-08-24
On 2022-08-24 the FDA classified a Class II recall of NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5" by Stradis Medical, citing the sterile barrier may be compromised.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1554-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-07-25 |
| Published | 2022-08-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stradis Medical |
| Distribution | US |
Product
NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701
Reason
The sterile barrier may be compromised.
Identifiers
| code_info | SKU/Part Number: ZZ-0701; Lots: 22027483172 and 22131487071 UDI/DI: M752ZZ07010 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1554-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.