Propaq LT vital signs monitor, Model 802LTON
This recall has been terminated (originally issued November 28, 2006).
- Company
- Welch Allyn Protocol, Inc
- Recall Initiated
- October 22, 2006
- Posted
- November 28, 2006
- Terminated
- August 2, 2011
- Recall Number
- Z-0215-2007
- Quantity
- total of both models 1031
- Firm Location
- Beaverton, OR
- Official Source
- View on FDA website ↗
Reason for Recall
Potential to burn patient's finger. A Nellcor pulse oximetry (Sp02) sensor became hot when used with a Propaq LT.
Distribution
Devices were distributed to hospitals/medical centers and dealers worldwide.
Lot / Code Info
KA001225 through KA002847
Root Cause
Other
Action Taken
A letter dated October 22, 2006 was sent to customers between October 25-27,2006. The letter advised of the problem and requested the customer contact the firm to arrange for return of the monitor to be serviced. The customer will be provided with a temporary replacement. The dealers were requested to notify their customers.
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