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Physio-Control, Inc.: LIFEPAK 15 (LP15)

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Due to an out of tolerance tool being used on monitor/defibrillator systems.. Recalled by Physio-Control, Inc.. Distribution: U.S.: CT, GA, MA, NY, OH, WA, and WV. O.U.S.: N/A. Classification (Class II — potential health risk). Affected lots/dates: LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 o 99577-000061 o 99577-000076 o 99. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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