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AirLife

Carefusion Corporation · Model 2K80253 · UDI-DI 10885403187384

OEV Prescription
0
510(k) clearances
197
Adverse events (19 deaths)
36
Recalls
18
Facilities

Description

1/2 Liter Neoprene Flow-Inflating Bag with Pre-Attached 7’ (2.1 m) Oxygen Tubing, Manometer and Infant Valved Mask

Recalls

DateFirmReason
2020-05-19ROi CPS LLCRoi CPS, LLC has become aware of a labeling error that affects select custom procedure kits. The kits are labeled with an expiration date that is later than that of the soonest kit
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab
2017-04-27Vyaire MedicalThe mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unab

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.