Recall Z-2130-2017— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2017-04-21, terminated 2020-01-27. FDA's recall record names no specific 510(k) clearance for this event. Product: INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory.
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-04-21
- Terminated
- 2020-01-27
- Firm location
- Research Triangle Park, NC, United States
Product description
INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory
Data sourced from openFDA. This site is unofficial and independent of the FDA.