Recall Z-1085-2020— Centurion Medical Products Corporation
Class II · Terminated
Class II FDA medical device recall by Centurion Medical Products Corporation, initiated 2019-12-11, terminated 2020-09-04. FDA's recall record names no specific 510(k) clearance for this event. Product: Centurion- Port Draw Kit KNV30 PORT DRAW KIT. Reason: Incomplete seals on the sterile package may compromise the sterility.
- Recalling firm
- Centurion Medical Products Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-12-11
- Terminated
- 2020-09-04
- Firm location
- Williamston, MI, United States
Product description
Centurion- Port Draw Kit KNV30 PORT DRAW KIT
Reason for recall
Incomplete seals on the sterile package may compromise the sterility
Data sourced from openFDA. This site is unofficial and independent of the FDA.