Abbott Laboratories, Inc: Medical Device Recalls in 2017

According to to data from the FDA, there were 3 medical device recalls made by Abbott Laboratories, Inc in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

• ARCHITECT c4000 Cuvette Segment, List number 02P75-01. The firm name on the label is Abbott Laboratories, Abbott Park, IL. Cuvette segments are a component to the ARCHITECT c4000 system. Cuvette segments are racks that sit in the reaction carousel and hold cuvettes. Each cuvette segment holds 11 cuvettes. With 9 segments, the reaction carousel holds 99 cuvettes. The Abbott ARCHITECT System is intended for In Vitro diagnostic use only. The system is designed to perform automated chemistry tests, utilizing photometry and potentiometric technology.
• ARCHITECT c4000 part number 02P24; ARCHITECT c8000 part number 01G06; ARCHITECT c16000 part number 03L77 Clinical Chemistry systems.
• Tubing, Peristaltic Head Part Number 7-35009685-01 for use in clinical chemistry systems.