Respire Pink+ Hard/Soft Oral Sleep Apnea Device recall
Respire Pink+ Hard/Soft Oral Sleep Apnea Device
Why was Respire Pink+ Hard/Soft Oral Sleep Apnea Device recalled?
Potential for device breakage during use
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial Numbers: 51366, 51439, 51368, 51577, 51303, 52409, 51985, 51796, 51709, 51744, 51560, 51321, 51545, 51437, 51571, 51576, 51438, 51566, 51509, 51629, 51502, 51409, 51307, 51218, 51154, 51001, 51220, 51153 & 50807
- Product
- Respire Pink+ Hard/Soft Oral Sleep Apnea Device
- Recalling firm
- Respire Medical
- Quantity
- 29 units
- Distribution
- US nationwide distribution.
- Recall date
- June 6, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)