Z-0344-2020 Class II Terminated
FDA device recall Z-0344-2020 was initiated by Centurion Medical Products Corporation on October 24, 2019 and is designated Class II. Reason for recall: Sterile packaging incomplete seals may compromise sterility of the product The recall status is terminated (terminated June 24, 2020). Affected quantity: 80 units.
Recall Details
- Product Type
- Devices
- Report Date
- November 13, 2019
- Initiation Date
- October 24, 2019
- Termination Date
- June 24, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 80 units
Product Description
Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG Code: DT11955
Reason for Recall
Sterile packaging incomplete seals may compromise sterility of the product
Distribution Pattern
Nationwide
Code Information
Lot/Batch Number: 2019052190 Exp Date: 5/31/2024