Z-2696-2024 Class II Ongoing
FDA device recall Z-2696-2024 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Mar 22, 2024 and is designated Class II. Reason for recall: A slight dimensional variation which has the potential for increased difficulty fitting into outer canister. The recall status is ongoing.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 28, 2024
- Initiation Date
- Mar 22, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K
Reason for Recall
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Distribution Pattern
Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
Code Information
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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2696-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026