Recall Z-2244-2017— ConvaTec, Inc
Class II · Terminated
Class II FDA medical device recall by ConvaTec, Inc, initiated 2017-05-10, terminated 2021-08-27. FDA's recall record names no specific 510(k) clearance for this event. Product: Non-Rebreather Mask w 7 (2.1 m) No-Crush Tubing, Adult, Product Code 9106-E, Product Code 9108-E, Product Code ZRNRMA.
- Recalling firm
- ConvaTec, Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-05-10
- Terminated
- 2021-08-27
- Firm location
- Greensboro, NC, United States
Product description
Non-Rebreather Mask w 7 (2.1 m) No-Crush Tubing, Adult, Product Code 9106-E, Product Code 9108-E, Product Code ZRNRMA
Data sourced from openFDA. This site is unofficial and independent of the FDA.