Recall Z-2236-2017— 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: Rebreather Oxygen Mask, Adult 7 (2.1 m) Tubing, Product Code 3104MM, Product Code 9104-E, Product Code PMD06001.
- 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
Rebreather Oxygen Mask, Adult 7 (2.1 m) Tubing, Product Code 3104MM, Product Code 9104-E, Product Code PMD06001
Data sourced from openFDA. This site is unofficial and independent of the FDA.