Z-0754-2024 Class II Terminated
FDA device recall Z-0754-2024 was initiated by Cardinal Health 200, LLC on Dec 21, 2023 and is designated Class II. Reason for recall: The above-listed lots of Cardinal Health Medi-Vac CRD" Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with… The recall status is terminated (terminated Oct 9, 2026). Affected quantity: 3505730 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jan 24, 2024
- Initiation Date
- Dec 21, 2023
- Termination Date
- Oct 9, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3505730 units
Product Description
CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510
Reason for Recall
The above-listed lots of Cardinal Health Medi-Vac CRD" Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with the outer hard canister.
Distribution Pattern
US, Canada, Australia and New Zealand
Code Information
UDI/DI 50630140152649 (case), Lot Numbers: J308-602, J308-605, J308-609, J308-623, J308-624, J308-625, J308-628, J308-629, J308-630, J308-632, J308-633, J308-634, J308-635, J308-636, J308-637, J308-640, J308-642, J308-607, J308-643, J309-603, J309-607, J309-623, J309-627, J309-630, J309-632, J309-635, J309-636, J309-637, J310-601, J310-609, J310-621, J310-622, J310-626, J310-627, J310-641, J310-642, J310-643, J310-644
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0754-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026