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.
This recall has been terminated (originally issued January 13, 2017).
- Company
- Teleflex Medical
- Recall Initiated
- January 13, 2017
- Terminated
- February 10, 2025
- Recall Number
- Z-1519-2017
- Quantity
- 7,600 eaches
- Firm Location
- Research Triangle Park, NC
- Official Source
- View on FDA website ↗
Reason for Recall
Labeling error
Distribution
Worldwide Distribution - US Nationwide in the state of AZ, CA, CO, CT, FL, GA, IL, IN, KY, LA, MD, MA, MI, MN, MS, MO, NV, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, WI, and the countries of Canada and Mexico.
Lot / Code Info
Lot/Batch Numbers 16A14 and 16A14
Root Cause
Unknown/Undetermined by firm
Action Taken
Consignees were notified of the recall by letter on 1/13/2017. The letter requested that they immediately discontinue use and quarantine the recalled product. Distributors were requested to conduct a sub-recall. The letter included a reply form which was to be returned to Teleflex.
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