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PEROUSE MEDICAL Recalls
4 recalls on record · July 30, 2014 to May 10, 2017 · Medical Devices
Recalls by year
14
15
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 10, 2017Medical DevicesFDA
PEROUSE MEDICAL recalls DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE N
Hazard: Complaints regarding broken blister.
January 7, 2015Medical DevicesFDA
PEROUSE MEDICAL recalls Synthes Inflation System (03.804.4135) Product Usage: Inflation system is used during kyphoplasty or other interven
Hazard: Additional instructions for use due to inability to raise the pressure above 10 atm during inflation phase may result in an incomplete inflation or delay in procedure
January 7, 2015Medical DevicesFDA
PEROUSE MEDICAL recalls Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended for use during cardiovascular to cr
Hazard: Additional instructions for use due to inability to raise the pressure above 10 atm during inflation phase may result in an incomplete inflation or delay in procedure
July 30, 2014Medical DevicesFDA
Perouse Medical recalls Perouse Flamingo, Model 0218TA and 0218TB intended for use during cardiovascular procedure to create, maintain and monit
Hazard: Perouse Medical in France initiated a voluntary recall of certain batches of Perouse FLAMINGO Inflations Devices due to a potential water-tightness default. The potential default could cause an air entry when the plunger is positioned around 20 mL.