FDA Device recall Z-2696-2024
1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K
- FDA Device
- Class II
- ongoing
- Published 2024-08-28
On 2024-08-28 the FDA classified a Class II recall of 1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K 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-2696-2024 |
| 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
1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K
Reason
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Identifiers
| code_info | UDI/DI 40888277276223 (package), 10888277276222 (unit), Lot Numbers: 670220510, 670220607, 670220607, 670220701, 67022…UDI/DI 40888277276223 (package), 10888277276222 (unit), Lot Numbers: 670220510, 670220607, 670220607, 670220701, 670220701, 670220701, 670220727, 670220721, 670220727, 670220727, 670220825, 670220825, 670221115, 670220915, 670220825, 670220915, 670220915, 670220928, 670220928, 670220928, 670221024, 670220928, 670221024, 670221220, 670221220, 670221124, 670221124, 670221213, 670221202, 670221202, 670221222, 670221222, 670221222, 670230206, 670230206, 670230215, 670230417, 670230331, 670230417, 670230508, 670230922, 670230922, 670231019, 670231101, 670231101, 670231123, 670231123, 670231116, 670231205 |
|---|
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-2696-2024%22
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