RecallRadar

FDA Device recall Z-2232-2017

Oxygen Masks, Elongated (Under Chin), Adult High Conc., Non-Rebreather, 7ft O2 Tubing, Check Valve, Two Side Valve, Product Code 108-E

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, Two Side Valve, Product Code 108-E by Convatec.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2232-2017
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 Masks, Elongated (Under Chin), Adult High Conc., Non-Rebreather, 7ft O2 Tubing, Check Valve, Two Side Valve, Product Code 108-E

Reason

Identifiers

code_info
Lot Number 100454, 100734, 101053, 101121, 101607, 101665, 101999, 102352, 102726, 102766, 102785, 103179, 103254, 103…Lot Number 100454, 100734, 101053, 101121, 101607, 101665, 101999, 102352, 102726, 102766, 102785, 103179, 103254, 103529, 104103, 104457, 104653, 104706, 104799, 105213, 105283, 105315, 105451, 105676, 109186

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-2232-2017%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.