medical MODERATE Updated 2017-06-14

ConvaTec, Inc recalls Non-Rebreather Mask w 7 (2.1 m) No-Crush Tubing, Adult, P

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Recalled Product

Non-Rebreather Mask w 7 (2.1 m) No-Crush Tubing, Adult, Product Code 9106-E, Product Code 9108-E, Product Code ZRNRMA

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Issued by

FDA

Affected States: CA, CT, FL, GA, IL, MO, NJ, NY, NC, OH, PA, RI, VA
Lot/Code Info: Lot Number (Product Code 9106-E) 100168, 101193, 101896; (Product Code 9108-E) 102143, 103119, 103378, 104273, 104839, 104879, 105224; (Product Code ZRNRMA) 101060, 103355, 104768, 105655

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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