Animas Recalls
6 recalls on record · October 10, 2012 to February 11, 2015 · Medical Devices
Recalls by year
12
13
14
15
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 11, 2015Medical DevicesFDA
Animas Corporation recalls Animas Vibe Insulin Infusion Pump. This product is indicated for continuous subcutaneous infusion of insulin for the
Hazard: Calibration factors in the pump overwritten during a programming step. The force sensor could send a lower signal value to the pump processor, with loss of prime warnings, occlusion alarms and the pump unable to detect a cartridge during the prime sequence. Field action initiated 8/29/2011.
November 5, 2014Medical DevicesFDA
Animas Corporation recalls Animas Vibe Insulin Infusion Pump and System. These products are indicated for continuous subcutaneous infusion of in
Hazard: Animas determined that keypad wear over time was contributing to an increased complaint rate associated with damaged keypads on the Vibe Insulin Infusion Pump and System. Animas has implemented an improvement to the keypad related to the material used to reduce susceptibility to damage and increase durability.
November 5, 2014Medical DevicesFDA
Animas Corporation recalls Animas Vibe Insulin Infusion Pump. This product is indicated for continuous subcutaneous infusion of insulin for the
Hazard: Animas determined that the Hebrew language translation in the Vibe Insulin Infusion Pump was incorrect and could lead to potential patient confusion. In addition, one line of Hebrew text was omitted from the display screen.
April 10, 2013Medical DevicesFDA
Animas Corporation recalls Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion o
Hazard: Animas has identified a component issue affecting a small supply of the Animas(R) 2020 insulin pumps. The component issue may trigger the pumps to sound a false alarm or warning related to one of the following: - Loss of prime; -Occlusion; or -No cartridge detected.
February 27, 2013Medical DevicesFDA
Animas Corporation recalls Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous subcut
Hazard: Due to an internal calendar date limit (December 31, 2015) these pumps will cease to operate on January 1, 2016, and will result in a call service alarm that is displayed on the pump display.
October 10, 2012Medical DevicesFDA
Animas Corporation recalls IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is inte
Hazard: Wear of the keypad that may lead to damage such as tearing or peeling of the edge of the keypad from the pump.