Non-Rebreather Mask w 7 — Class II medical device recall Z-2244-2017
Terminated recall by ConvaTec, Inc, reported 2017-06-14, distributed in CA, CT, FL, GA, IL, MO, NC, NJ….
| Recall number | Z-2244-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ConvaTec, Inc, Greensboro, NC, United States |
| Recall initiated | 2017-05-10 |
| Classified | 2017-06-02 |
| Reported by FDA | 2017-06-14 |
| Terminated | 2021-08-27 |
| Distributed | CA, CT, FL, GA, IL, MO, NC, NJ, NY, OH, PA, PR, RI, VA |
| Countries outside the US | AU, BE, CA, CH, CZ, DE, DK, FI, FR, GB, GR, IL, IT, JO, JP, MT, MY, NL, NO, SA, SE, VN |
| Lot numbers | 100168, 101060, 101193, 101896, 102143, 103119, 103355, 103378, 104273, 104768, 104839, 104879, 105224, 105655 |
Product
Non-Rebreather Mask w 7 (2.1 m) No-Crush Tubing, Adult, Product Code 9106-E, Product Code 9108-E, Product Code ZRNRMA
Reason for recall
Not stated by FDA.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2244-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.