Z-1090-2020 Class II Terminated
FDA device recall Z-1090-2020 was initiated by Centurion Medical Products Corporation on December 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 September 4, 2020). Affected quantity: 108 units.
Recall Details
- Product Type
- Devices
- Report Date
- February 12, 2020
- Initiation Date
- December 11, 2019
- Termination Date
- September 4, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 108 units
Product Description
Centurion- Skin Prep Kits SB1280 SKIN SCRUB KIT SB1525 VAGINAL PREP TRAY
Reason for Recall
Incomplete seals on the sterile package may compromise the sterility
Distribution Pattern
Nationwide Foreign: GHANA
Code Information
Product/Description/Lot Numbers: SB1280 SKIN SCRUB KIT 2018112690 SB1525 VAGINAL PREP TRAY 2018103190