Recall Z-1093-2018— Centurion Medical Products Corporation
Class II · Terminated
Class II FDA medical device recall by Centurion Medical Products Corporation, initiated 2017-10-23, terminated 2018-06-21. FDA's recall record names no specific 510(k) clearance for this event. Product: IV START KIT. Reason: Convenience Kit containing components to assist practitioner with IV placement and securement..
- Recalling firm
- Centurion Medical Products Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-10-23
- Terminated
- 2018-06-21
- Firm location
- Williamston, MI, United States
Product description
IV START KIT
Reason for recall
Convenience Kit containing components to assist practitioner with IV placement and securement.
Data sourced from openFDA. This site is unofficial and independent of the FDA.