International safety notice

Terumo

United Kingdom / MHRA · GBR · Dec 1, 2018

Key facts

Title Terumo
Regulator United Kingdom / MHRA
Country GBR
Brand Trima Accel Automated Blood Collection System
Manufacturer Terumo
Event type Safety Notice
Action type Field safety notice
Medical specialty Anaesthetics, Cardiology, Care home staff, Cosmetic surgery, Critical care, Dentistry, General practice, General surgery, Haematology and oncology, Infection prevention, Obstetrics and gynaecology, Ophthalmology, Orthopaedics, Paediatrics, Pathology, Pharmacy, Physiotherapy and occupational therapy, Radiology, Renal medicine, Theatre practitioners, Urology, Vascular and cardiac surgery
Date Dec 1, 2018
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

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