FDA recall record

Stryker Medical Division of Stryker T/Pump temperature therapy pump, Models TP700 and TP700C recall — FDA Z-1013-2018

The T/Pump Operations Manual and Maintenance Manual were incorrectly revised to add the sentence, Temperature therapy can also be for heat conservation…

Class IIIclassification
Z-1013-2018official record ID
Mar 21, 2018report date

Recall record at a glance

Official recordZ-1013-2018
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmStryker Medical Division of Stryker Corporation
Report dateMar 21, 2018
Recall initiation dateNov 7, 2017
Quantity9902
LocationPortage, MI, United States

Official product description

T/Pump temperature therapy pump, Models TP700 and TP700C

Why the product was recalled

The T/Pump Operations Manual and Maintenance Manual were incorrectly revised to add the sentence, Temperature therapy can also be for heat conservation for normothermia maintenance to the Indications for Use statement.

Distribution information

Distributed in all 50 states, the District of Columbia, and Guam.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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