FDA Device recall Z-1033-2023
Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case
- FDA Device
- Class II
- ongoing
- Published 2023-02-08
On 2023-02-08 the FDA classified a Class II recall of Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case by Medline Industries Northfield, citing potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1033-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-11-17 |
| Published | 2023-02-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case
Reason
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
Identifiers
| code_info | Item Number: DYNJ908295, UDI/GTIN Case: 40195327029570, UDI/GTIN Each: 10195327029579, Lot Numbers: 22IBN449, 22JBQ931 |
|---|
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-1033-2023%22
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