Respire Medical recalls

Respire Medical has 5 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 6 Jun 2018. The most frequent reason is device malfunction.

Total recalls5since 2018

Last 12 months0reported

Class I00% of total

Ongoing0latest 6 Jun 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 5 100%Class III 0 0%

Why respire medical is recalled

Device Malfunction5100%

Product types

Other Medical Devices5100%

By year

20185100%

All respire medical recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
6 Jun 2018Device	CLASS II	Respire Pink+ Hard Oral Sleep Apnea Device recalled by Respire Medical	Respire Medical	Device Malfunction	Nationwide
6 Jun 2018Device	CLASS II	Respire Pink+ Hard/Soft Oral Sleep Apnea Device recalled	Respire Medical	Device Malfunction	Nationwide
6 Jun 2018Device	CLASS II	Respire Pink H/S Oral Sleep Apnea Device recalled by Respire Medical	Respire Medical	Device Malfunction	Nationwide
6 Jun 2018Device	CLASS II	Respire Pink H/S Oral Sleep Apnea Device recalled by Respire Medical	Respire Medical	Device Malfunction	Nationwide
6 Jun 2018Device	CLASS II	Respire Pink Series EF+ Oral Sleep Apnea Device recalled	Respire Medical	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.