LMA ATOMIZATION IPN049182Recalls & reported problems
Teleflex Incorporated · MAD Nasal without Syringe · Class 1
All models of LMA ATOMIZATION (5)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704626547), received between Oct 3, 2023 and Oct 3, 2023 — classified as 1 malfunction.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 3, 2023
INTRANASAL MUCOSAL ATOMIZATION DEVICE NOT WORKING PROPERLY. WHEN IN USE, IT SPRAYS A STREAM RATHER THAN ATOMIZING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17860581 ↗
Other NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER) devices
- LMA ATOMIZATION IPN915303Teleflex Incorporated · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)18 reports
- LMA ATOMIZATION IPN048826Teleflex Incorporated · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)11 reports
- Salter AIRE Elite 8350-8900Salter Labs · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)8 reports
- Salter AIRE Elite SO-1774BESalter Labs · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)7 reports
- N/A 8904-7Salter Labs · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)5 reports
- AirLife™ 441HAirlife · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)1 report
- HUDSON RCI IPN049826Teleflex Incorporated · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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