RecallRadar

FDA Device recall Z-2239-2017

Oxygen Mask, Elongated (Under the Chin) Pediatric, High Concentration Rebreather, 7 ft. (2.1 m) Oxygen Tubing w/FITS-All Oxygen Connector,…

On 2017-06-14 the FDA classified a Class II recall of Oxygen Mask, Elongated (Under the Chin) Pediatric, High Concentration Rebreather, 7 ft. (2.1 m) Oxygen Tubing w/FITS-All Oxygen Connector,… by Convatec.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2239-2017
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

Oxygen Mask, Elongated (Under the Chin) Pediatric, High Concentration Rebreather, 7 ft. (2.1 m) Oxygen Tubing w/FITS-All Oxygen Connector, Product Code 3224-E and Product Code 3226-E

Reason

Identifiers

code_info
Lot Number  (Product Code 3224-E) 105215; (Product Code 3226-E) 100497, 100748, 101140, 102282, 102400, 102727, 102858…Lot Number  (Product Code 3224-E) 105215; (Product Code 3226-E) 100497, 100748, 101140, 102282, 102400, 102727, 102858, 103188, 103273, 103300, 103853, 104081, 104654, 104889, 105065, 105190, 105216, 13-34

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-2239-2017%22

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