Recall Z-0344-2020— Centurion Medical Products Corporation
Class II · Terminated
Class II FDA medical device recall by Centurion Medical Products Corporation, initiated 2019-10-24, terminated 2020-06-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG Code: DT11955. Reason: Sterile packaging incomplete seals may compromise sterility of the product.
- Recalling firm
- Centurion Medical Products Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-10-24
- Terminated
- 2020-06-24
- Firm location
- Williamston, MI, United States
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.