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Infinity Delta Portable Patient Monitor. Draeger Medical Systems, Inc. Portable monitor used to monitor vital signs of n

FDA device recall Z-3047-2011 · posted 2011-08-22 · Terminated

Recall details

Recalling firm
Draeger Medical Systems, Inc.
Reason for recall
Monitor keys may spontaneously become inoperative or active. This may cause a membrane switch panel malfunction, which could result in the monitor discharging a patient automatically.
Action taken
Draeger Medical sent an "Urgent Medical Device Recall Notification" letters dated July 2011 to all affected customers. The letter included product and problem affected. The letter informed the customer a Draeger representative will contact them to upgrade the system. Until the solution is implemented, Draeger recommends the Delta and/or Gamma XXL may be used. If the affected monitors become inoperative or activate without user interaction, Draeger advises removing the monitor from service and contacting a Draeger representative. For questions or for information on this recall please call Draeger Service at (800) 543-5047 (press 1 at the prompt, then 2, then 32349).
Root cause
Device Design
Status
Terminated
Product code
MHX
Quantity affected
32
Distribution
Worldwide Distribution - (USA) Nationwide distribution including the states of AK, FL, LA, MN, MS, MO, NJ, NC, OH, OK, PA, TN, TX, NC, NH, NJ, NY, WV, and WI; and the countries of Australia, Austria,
Date initiated
2011-07-29
Date posted
2011-08-22
Date terminated
2012-08-16
Location
Telford, PA

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Related 510(k) clearances

RecordFirmDate
INFINITY DELTA/DELTA XL/ KAPPA/ GAMMA X XL/ VISTA XL/ SC7000/SC8000/ SC9000XL (K070566)Draeger Medical Systems, Inc.2007-06-04