FDA Device recall Z-2366-2023
Total Hip Kit, REF DYNJ903275S
- FDA Device
- Class II
- ongoing
- Published 2023-08-16
On 2023-08-16 the FDA classified a Class II recall of Total Hip Kit, REF DYNJ903275S by Medline Industries Northfield, citing the prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2366-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-07-03 |
| Published | 2023-08-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Total Hip Kit, REF DYNJ903275S; surgical convenience kit
Reason
The prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit.
Identifiers
| code_info | UDI/DI: 10195327254582 (unit), 40195327254583 (case); Lot code 23CDC733 |
|---|
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-2366-2023%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.