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Recall Observatory FDA recall evidence

Device product

ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff. The system is intended for use only in professional healthcare facilities. It is not intended to be used in the home healthcare environment.

Z-2714-2017

June 14, 2017

Class II

Product summary

Firm
Arjo, Inc. dba ArjoHuntleigh
Event
Event 77551
Status
Terminated
Classification
Class II
Quantity
40,675 units worldwide
Official record key
device-enforcement:Z-2714-2017

Official wording

Reason: Reports of the device failure involving delivering continuous pressure to the calf garment and not deflating as intended, without triggering an alarm.

Code information: Model numbers: 526000-01, 526000-01P, 526000-02, 526000-02P. Serial numbers range from 1400028031 to 1600048470.

Distribution pattern: Worldwide Distribution - US (Nationwide) and internationally to the following countries: United Kingdom, Australia, New Zealand, Japan, Italy, United Arab Emirates, France, Canada, Brazil, Austria, Saudi Arabia, Qatar, India, Switzerland, Bahrain, Kuwait, South Africa, Lebanon, Netherlands, Poland, Spain, Ecuador, Hong-Kong, Colombia, Malaysia, Paraguay, Mauritius, Cyprus, Greece, Oman, Norway, Ireland, Pakistan, Czech Republic, Mexico, Sweden, Tanzania, Hungary, Singapore, Jordan, Israel, Denmark, Chile, and Germany.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports of the device failure involving delivering continuous pressure to the calf garment and not deflating as intended, without triggering an alarm.