Reported Jun 6, 2018 · Terminated

Respire Pink+ Hard Oral Sleep Apnea Device

Respire Medical

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Respire Medical · 18 Bridge St Ste 4J · Brooklyn, NY · 11201-1107

Is this the product you have?

  • Respire Pink+ Hard Oral Sleep Apnea Device
Lot codes and dates
  • Serial Numbers
    • 51447
    • 51460
    • 51612
    • 51318
    • 51320
    • 51839
    • 51714
    • 51909
    • 51720
    • 51397
    • 51498
    • 51413
    • 51581
    • 51479
    • 51503
    • 51496
    • 51163
    • 51084
    • 50472
    • 46747
    • 46125
    • 46000
    • 46101
    • 46268 & 52634
Amount recalled
25 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for device breakage during use

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 9, 2019 · Data as of Sep 19, 6:14 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.