Data Foundry

Medical device recalls 2017

Non-Rebreathing Mask — Class II medical device recall Z-2230-2017

Terminated recall by ConvaTec, Inc, reported 2017-06-14, distributed in CA, CT, FL, GA, IL, MO, NC, NJ….

Recall numberZ-2230-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmConvaTec, Inc, Greensboro, NC, United States
Recall initiated2017-05-10
Classified2017-06-02
Reported by FDA2017-06-14
Terminated2021-08-27
DistributedCA, CT, FL, GA, IL, MO, NC, NJ, NY, OH, PA, PR, RI, VA
Countries outside the USAU, BE, CA, CH, CZ, DE, DK, FI, FR, GB, GR, IL, IT, JO, JP, MT, MY, NL, NO, SA, SE, VN
Lot numbers100152, 100232, 100694, 100720, 100918, 101141, 101639, 101897, 102095, 102154, 103067, 103122, 103159, 103385, 103527, 103558, 104009, 104321, 104322, 104328, 1045675, 104701, 104846, 104848, 104975, 105453, 105569, 105656

Product

Non-Rebreathing Mask, Reservoir Bag, Check Valve, One Side Valve, with Tubing, Product Code 106-E, Product Code 3226MM, and Product Code 9108MM

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-2230-2017. 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.