Z-1093-2020 Class II Terminated
FDA device recall Z-1093-2020 was initiated by Centurion Medical Products Corporation on Dec 11, 2019 and is designated Class II. Reason for recall: Incomplete seals on the sterile package may compromise the sterility The recall status is terminated (terminated Sep 4, 2020). Affected quantity: 420 units.
Recall Details
- Product Type
- Devices
- Report Date
- Feb 12, 2020
- Initiation Date
- Dec 11, 2019
- Termination Date
- Sep 4, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 420 units
Product Description
Centurion- PT225 PAIN MANAGEMENT TRAY
Reason for Recall
Incomplete seals on the sterile package may compromise the sterility
Distribution Pattern
Nationwide Foreign: GHANA
Code Information
Lot Number: 2019021490
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1093-2020
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026