PlainRecalls
FDA Devices Moderate Class II Terminated

Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and aid placement of a tracheal tube.

Reported: August 6, 2014 Initiated: July 9, 2014 #Z-2119-2014

Product Description

Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and aid placement of a tracheal tube.

Reason for Recall

Packaging Error: Customers have reported receiving incorrect product. The box labeling indicates the correct product MAC 4 but the contents are incorrect, Miller 4 blades.

Details

Recalling Firm
Teleflex Medical
Units Affected
120 units
Distribution
US Distribution including the states of FL, GA, KY, MD, MS, MT, PA, SC and TX.
Location
Durham, NC

Frequently Asked Questions

What product was recalled?
Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and aid placement of a tracheal tube.. Recalled by Teleflex Medical. Units affected: 120 units.
Why was this product recalled?
Packaging Error: Customers have reported receiving incorrect product. The box labeling indicates the correct product MAC 4 but the contents are incorrect, Miller 4 blades.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 6, 2014. Severity: Moderate. Recall number: Z-2119-2014.