Z-2698-2024 Class II Ongoing
FDA device recall Z-2698-2024 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. Affected quantity: 35900 units.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 28, 2024
- Initiation Date
- Mar 22, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 35900 units
Product Description
1,5L MED-SOFT LINER W/ 6MMX3M TUB. & ADULT VC, REF OR53929
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 40888277422286 (package), 0888277DC265NSKX (unit), Lot Numbers: 670220505, 670220609, 670220621, 670220720, 670220804, 670220926, 670220928, 670221024, 670221115, 670221227, 670230109, 670230210, 670230424
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2698-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026