FDA-Device2018-06-06Class II

Respire Pink Series EF+ Oral Sleep Apnea Device.

Respire Medical
Hazard

Potential for device breakage during use

Sold states
US nationwide distribution.
Affected count
1 unit
Manufactured in
18 Bridge St Ste 4J, N/A, Brooklyn, NY, United States
Products
Respire Pink Series EF+ Oral Sleep Apnea Device.

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1947-2018

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief