Z-1015-2023 Class II Ongoing
FDA device recall Z-1015-2023 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Dec 23, 2022 and is designated Class II. Reason for recall: The kit contained an expired component. The recall status is ongoing. Affected quantity: 1050 kits.
Recall Details
- Product Type
- Devices
- Report Date
- Feb 1, 2023
- Initiation Date
- Dec 23, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1050 kits
Product Description
CENTURION MEDICAL PRODUCTS, SILVER ANTIMICROBIAL VAD DRIVE, REF DT18760
Reason for Recall
The kit contained an expired component.
Distribution Pattern
US Nationwide distribution in the states of NY, IN, FL, NJ, IL.
Code Information
UDI/DI 10653160274841, Lot Numbers 22ABO498
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1015-2023
- openFDA file date
- Oct 21, 2026
- Loaded by RegDataLab
- Oct 23, 2026