FDA Device recall Z-1280-2022
Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A
- FDA Device
- Class II
- ongoing
- Published 2022-06-29
On 2022-06-29 the FDA classified a Class II recall of Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A by New Standard Device, citing due to manufacturing processing error, wrench causing stripping when torqueing nuts.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1280-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-08-14 |
| Published | 2022-06-29 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | New Standard Device |
| Distribution | AZ, CT, GA, OH, VA |
Product
Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A
Reason
Due to manufacturing processing error, wrench causing stripping when torqueing nuts.
Identifiers
| code_info | Catalog/Part Number: 900104 UDI-DI (GTIN): 854641008112 Lot Number: A29618A |
|---|
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-1280-2022%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.