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LMA
TELEFLEX INCORPORATED · Model IPN046399 · UDI-DI 05060112313233
CCT
Prescription
1
510(k) clearances
26
Adverse events
6
Recalls
5
Facilities
Description
Pediatric Laryngo-Tracheal Mucosal Atomization Device with 5ml Syringe
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-03-19 | Teleflex Medical Europe Ltd | Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label. |
| 2017-07-05 | Teleflex Medical | Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label. |
| 2016-10-27 | Teleflex Medical | Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication. |
| 2009-03-05 | Sharn, Inc. | Sharn Anesthesia Inc., Tampa, FL received reports of leaking containers following use of their Sharn Anesthesia Microblast nasal and pediatric laryngeal atomizer device. |
| 2009-03-05 | Sharn, Inc. | Sharn Anesthesia Inc., Tampa, FL received reports of leaking containers following use of their Sharn Anesthesia Microblast nasal and pediatric laryngeal atomizer device. |
| 2009-03-05 | Sharn, Inc. | Sharn Anesthesia Inc., Tampa, FL received reports of leaking containers following use of their Sharn Anesthesia Microblast nasal and pediatric laryngeal atomizer device. |
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Get your free API keyRead the docsData 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.