FDA Device recall Z-2237-2017
Oxygen Masks, Elongated (Under Chin) Adult High Conc., Non-Rebreather, 7ft O2 Tubing, Check Valve, One Side Valve, FITS-All Conn., Product…
- FDA Device
- Class II
- terminated
- Published 2017-06-14
On 2017-06-14 the FDA classified a Class II recall of Oxygen Masks, Elongated (Under Chin) Adult High Conc., Non-Rebreather, 7ft O2 Tubing, Check Valve, One Side Valve, FITS-All Conn., Product… by Convatec.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2237-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-10 |
| Published | 2017-06-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Convatec |
| Distribution | CA, CT, FL, GA, IL, MO, NC, NJ, NY, OH, PA, PR, RI, VA |
Product
Oxygen Masks, Elongated (Under Chin) Adult High Conc., Non-Rebreather, 7ft O2 Tubing, Check Valve, One Side Valve, FITS-All Conn., Product Code 3106-E
Reason
Identifiers
| code_info | Lot Number 100272, 100465, 101132, 101616, 101994, 102398, 102788, 102935, 103192, 103384, 103445, 103851, 103908, 104…Lot Number 100272, 100465, 101132, 101616, 101994, 102398, 102788, 102935, 103192, 103384, 103445, 103851, 103908, 104078, 104902, 104947, 105189, 105441, 105935 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2237-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.