Z-0487-2024 Class II Ongoing
FDA device recall Z-0487-2024 was initiated by Remington Medical, Inc. on November 3, 2023 and is designated Class II. Reason for recall: There is an error with the "Use by Date" and "Date of Manufacturer" on the box label. The recall status is ongoing. Affected quantity: 3080 devices.
Recall Details
- Product Type
- Devices
- Report Date
- December 13, 2023
- Initiation Date
- November 3, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3080 devices
Product Description
Remington MEDICAL Drainage Bag, REF 600-D;
Reason for Recall
There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.
Distribution Pattern
US: PA and FL
Code Information
UDI/DI 20813079020008, Lot Number 2325111