Reported Mar 29, 2017 · Terminated

Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a…

Teleflex 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: Teleflex Medical · 2917 Weck Dr · Research Triangle Park, NC · 27709-0186

Is this the product you have?

  • Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130
  • and 123132 Product UsageTo provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx
Lot codes and dates
  • Lot/Batch Numbers 16A14 and 16A14
Amount recalled
7,600 eaches

Where it was sold

Why it was recalled

Labeling error

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 10, 2025 · Data as of Sep 19, 6:48 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.