Flowonix Medical Inc: Medical Device Recalls in 2020
Updated on March 25, 2026.
According to to data from the FDA, there were 6 medical device recalls made by Flowonix Medical Inc in 2020. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Prometra II Programmable 20mL Pump. Catalog No. 93827 The device is an implantable infusion pump. GTIN-14 00810335020YYY (YYY= in-country language specific)
- Prometra Programmable 20mL Pump. Catalog No. 11827 The device is an implantable infusion pump. GTIN-14 00810335020082
- US Clinical 20mL Programmable Pump. Catalog No. 01827 The device is an implantable infusion pump. GTIN-14 00810335020082
- Prometra II 40mL Pump. Catalog No. 16827 The device is an implantable infusion pump. GTIN-14 00810335020242
- Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion pump. GTIN-14 00810335020XXX (XXX = in-country language specific)
- Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN-14 00810335020228
Popular Topics:
Find us
Copyright © Beautify Data LLC. All Rights Reserved.