CLASS II Device recall · Reported 14 Jun 2017 · FDA Enforcement Report
Rebreathing Mask, Reservoir, with Tubing, Product recalled by ConvaTec
ConvaTec is recalling Rebreathing Mask, Reservoir, with Tubing, distributed in 14 states. The recall was initiated on 10 May 2017 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2229-2017
- FDA event ID
- 77282
- Recalling firm
- ConvaTec, Greensboro, NC
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 10 May 2017
- FDA classified
- 2 Jun 2017
- Reported
- 14 Jun 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Masks, Gloves & PPE
Timeline
| 10 May 2017 | Recall initiated by company | |
| 2 Jun 2017 | Classified by FDA | +23 days |
| 14 Jun 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Not stated in the enforcement report.
Product as listed by the FDA
Rebreathing Mask, Reservoir bag, with Tubing, Product Code 104MM
Where it was distributed
CA, CT, FL, GA, IL, MO, NJ, NY, NC, OH, PA, RI, VA , Puerto Rico, Australia, Belgium, Canada, Columbia, Czech, Denmark, Finland, France, Germany, Greece, Israel, Italy, Japan, Jordan, Malaysia, Malta, Netherlands, Norway, Rwanda, Saudi Arabia, Sweden, Switzerland, United Kingdom, and Vietnam
CaliforniaConnecticutFloridaGeorgiaIllinoisMissouriNorth CarolinaNew JerseyNew YorkOhioPennsylvaniaPuerto RicoRhode IslandVirginia
Questions about this recall
Why was it recalled?
The reason has not been published.
Which lots are affected?
Lot Number 105631
Where was it sold?
CA, CT, FL, GA, IL, MO, NJ, NY, NC, OH, PA, RI, VA , Puerto Rico, Australia, Belgium, Canada, Columbia, Czech, Denmark, Finland, France, Germany, Greece, Israel, Italy, Japan, Jordan, Malaysia, Malta, Netherlands, Norway, Rwanda, Saudi Arabia, Sweden, Switzerland, United Kingdom, and Vietnam
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
17 other products · FDA event 77282This product is part of a recall event; the main page for the event is Non-Rebreather Oxygen Mask, Adult High Concentration recalled.
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