medical MODERATE Updated 2017-03-29

Teleflex Medical recalls Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, C

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Recalled Product

Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx.

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Hazard / Issue

Labeling error

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot/Batch Numbers 16A14 and 16A14

✅ 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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