Z-2699-2024 Class II Ongoing
FDA device recall Z-2699-2024 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: 316125 units.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 28, 2024
- Initiation Date
- Mar 22, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 316125 units
Product Description
1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PG
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 20888277660103 (package), 0888277DC265NSKX (unit), Lot Numbers: 670220511, 670220622, 670220628, 670220706, 670220720, 670220801, 670220805, 670220907, 670220912, 670221020, 670221115, 670221128, 670221205, 670221213, 670221219, 670221223, 670230105, 670230213, 670230308, 670230322, 670230424, 670230530, 670230601
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2699-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026