Welch Allyn Protocol, Inc Propaq LT vital signs monitor, Model 802LTON Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Propaq LT vital signs monitor, Model 802LTON
Brand
Welch Allyn Protocol, Inc
Lot Codes / Batch Numbers
KA001225 through KA002847
Products Sold
KA001225 through KA002847
Welch Allyn Protocol, Inc is recalling Propaq LT vital signs monitor, Model 802LTON due to Potential to burn patient's finger. A Nellcor pulse oximetry (Sp02) sensor became hot when used with a Propaq LT.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential to burn patient's finger. A Nellcor pulse oximetry (Sp02) sensor became hot when used with a Propaq LT.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026