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Respire Medical recalls Respire Pink+ Hard Oral Sleep Apnea Device
Recalled June 6, 2018 · FDA recall Z-1949-2018 · Respire Medical
Hazard
Potential for device breakage during use · FDA Class II
Units
25 units
Sold at
US nationwide distribution.
Description
Potential for device breakage during use
Product
Respire Pink+ Hard Oral Sleep Apnea Device
Manufacturer(s)
Respire Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →