Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland
This page shows every FDA and USDA recall linked to Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
11
Total Recalls
2018
First Recall
2021
Most Recent
RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers:
a) 170050
b) 170055
c) 17...
Jul 16, 2021
· Device
Open, Classified
RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers:
a) 112082050
b)...
Jul 16, 2021
· Device
Open, Classified
RUSCH Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF numbers:
a) 112080050
b) 1120...
Jul 16, 2021
· Device
Open, Classified
RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers:
a) 504550
b) 504555
c)...
Jul 16, 2021
· Device
Open, Classified
Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542
Product Usage:
general surgical scissors
Jun 14, 2018
· Device
Terminated
Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50
Product Usage:
for use...
Apr 17, 2018
· Device
Terminated
Latex Rebreathing Bags:
Product Code Equivalent Code
(a) 151174050 151174
(b) 153000005 153000005
(c) 15300001...
Apr 12, 2018
· Device
Terminated
Baker Jejunostomy Tubes:
Product Code Equivalent Code
(a) 655300160 655316
(b) 655500200 655520
Apr 12, 2018
· Device
Terminated
Simplastic Suprapubic Puncture Instruments:
Product Code Equivalent Code
(a) 650704100 551310
(b) 65...
Apr 12, 2018
· Device
Terminated
Rectal Catheters;
Product Code Equivalent Code
580114 580114
Product Usage:
Rectal Balloon Cathet...
Apr 12, 2018
· Device
Terminated
Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for t...
Mar 19, 2018
· Device
Terminated