FDA Device recall Z-2710-2024
Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F
- FDA Device
- Class II
- ongoing
- Published 2024-08-28
On 2024-08-28 the FDA classified a Class II recall of Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F by Medline Industries Northfield, citing A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2710-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-22 |
| Published | 2024-08-28 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F
Reason
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Identifiers
| code_info | a) REF DYKC1289F, UDI/DI 40195327510917 (case), 10195327510916 (unit), Lot Numbers: 23LBF766 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2710-2024%22
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