PlainRecalls
FDA Devices Moderate Class II Terminated

Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Reported: August 5, 2020 Initiated: July 6, 2020 #Z-2732-2020

Product Description

Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

Reason for Recall

Breaking at the point of a welded joint

Details

Recalling Firm
TELEFLEX MEDICAL INC
Units Affected
29740 units
Distribution
US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.
Location
Morrisville, NC

Frequently Asked Questions

What product was recalled?
Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.. Recalled by TELEFLEX MEDICAL INC. Units affected: 29740 units.
Why was this product recalled?
Breaking at the point of a welded joint
Which agency issued this recall?
This recall was issued by the FDA Devices on August 5, 2020. Severity: Moderate. Recall number: Z-2732-2020.