FDA recall Z-0344-2020
Centurion Medical Products Corporation · Class II · device
Product
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
Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2019-10-24
- Report date
- 2019-11-13
- Termination date
- 2020-06-24
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Williamston, MI, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0344-2020