RecallRadar

FDA Device recall Z-2230-2017

Non-Rebreathing Mask, Reservoir Bag, Check Valve, One Side Valve, with Tubing, Product Code 106-E, Product Code 3226MM, and Product Code 91…

On 2017-06-14 the FDA classified a Class II recall of Non-Rebreathing Mask, Reservoir Bag, Check Valve, One Side Valve, with Tubing, Product Code 106-E, Product Code 3226MM, and Product Code 91… by Convatec.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2230-2017
ClassificationClass II
Statusterminated
Initiated2017-05-10
Published2017-06-14
Last updated2026-09-13 11:54 UTC
CompanyConvatec
DistributionCA, CT, FL, GA, IL, MO, NC, NJ, NY, OH, PA, PR, RI, VA

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

Identifiers

code_info
Lot Number (Product Code 106-E), 100152, 102095, 102154, 103122, 103159, 103385, 103527, 103558, 104009, 104321, 10432…Lot Number (Product Code 106-E), 100152, 102095, 102154, 103122, 103159, 103385, 103527, 103558, 104009, 104321, 104322, 104328, 104701, 104975, 105569, 105656, 1045675; (Product Code 3226MM) 100720, 101141; (Product Code 9108MM) 100232, 100694, 100918, 101639, 101897, 103067, 104846, 104848, 105453

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-2230-2017%22

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