Z-2694-2024 Class II Ongoing
FDA device recall Z-2694-2024 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
LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500
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 40884389129532 (package), 10884389129531 (unit), Lot Numbers: 670220523, 670220531, 670220613, 670220530, 670220624, 670220613, 670220704, 670220704, 670220624, 670220624, 670220713, 670220713, 670220727, 670220721, 670220804, 670220912, 670220916, 670220901, 670220916, 670220916, 670221013, 670221013, 670221013, 670221013, 670221026, 670221026, 670221103, 670221103, 670221103, 670221103, 670221103, 670221129, 670221207, 670221210, 670221224, 670221210, 670230103, 670230103, 670221210, 670230103, 670221210, 670230208, 670230208, 670230220, 670230220, 670230306, 670230313, 670230327, 670230327, 670230414, 670230422, 670230414, 670230427, 670230510, 670230518, 670230525, 670230925, 670230925, 670230925, 670231006, 670231020, 670231103, 670231103, 670231114, 670231201, 670231201, 670231127
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2694-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026