FDAFDA · Food and drugs·Recall number Z-1771-2013
Spacelabs ARKON Anesthesia Workstation. Spacelabs ARKON Anesthesia Workstation may be used for the delivery of oxygen, air and nitrous oxide in a controlled manner to various patient breathing circuits with or without the use of mechanical ventilator, and may be used for the delivery of anesthetic vapor by use of a dismountable vaporizer.
Published July 31, 2013 · Recall initiated: June 7, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Spacelabs ARKON Anesthesia System is recalled due to software defect. The System Status Computer may incorrectly determine that a communication error has occurred. If this situation occurs, a buzzer will activate and a yellow triangle will be displayed on the System Status Computer screen that alerts the user of this error.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Del Mar Reynolds Medical, Ltd.
- Distributor
- Worldwide Distribution - USA including South Carolina and internationally to Canada and Great Britian.
- Lot
- ARKN-000001, ARKN-000005, ARKN-000010, ARKN-000015, ARKN-000016, ARKN-000017, ARKN-000018, ARKN-000020, ARKN-000021.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United Kingdom
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