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Teleflex Medical recalls Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code
Recalled December 28, 2016 · FDA recall Z-0898-2017 · Teleflex Medical
Hazard
Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication. · FDA Class II
Units
2,674,650 units in total
Sold at
Worldwide distribution. U.S. (Nationwide) and Internationally to Canada, Belgium, Singapore and Thailand.
Description
Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
Product
Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code MAD100, MAD100OS MAD110, MAD110OS, MAD130, MAD130OS, MAD140, MAD140OS, MAD300, MAD300B. Manufactured By: Wolfe-Tory Medical, Inc., Teleflex Medical. For atomization of topical solutions across the naso and oropharyngeal mucosal membranes
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →