Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-1519-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: January 13, 2017

Date Posted: March 29, 2017

Recall Number: Z-1519-2017

Event ID: 76263

Reason for Recall:

Labeling error

Status: Terminated

Product Quantity: 7,600 eaches

Code Information:

Lot/Batch Numbers 16A14 and 16A14

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated