Recall Z-1519-2017— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2017-01-13, terminated 2025-02-10. FDA's recall record names no specific 510(k) clearance for this event. 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.. Reason: Labeling error.
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-01-13
- Terminated
- 2025-02-10
- Firm location
- Research Triangle Park, NC, United States
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.
Reason for recall
Labeling error
Data sourced from openFDA. This site is unofficial and independent of the FDA.