Recall Z-2233-2017— 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 Oxygen Mask, Adult High Concentration with 2.1 m (7) Oxygen Tubing, Product Code 108MM.
- 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 Oxygen Mask, Adult High Concentration with 2.1 m (7) Oxygen Tubing, Product Code 108MM
Data sourced from openFDA. This site is unofficial and independent of the FDA.