Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Thumper Cardiopulmonary Resuscitator Recalled by Michigan Instruments, Inc. Due to A performance issue with the chest depth needle...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Michigan Instruments, Inc. directly.
Affected Products
Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370 Product Usage: The device is used to perform Cardiopulmonary Resuscitation (CRP) on adult patients and only adult patients in cases of clinical death as defined by a lack of spontaneous breathing and pulse.
Quantity: 38 devices
Why Was This Recalled?
A performance issue with the chest depth needle valve (CDNV) may arise where turning the knob will not deliver any compression depth to the piston during the first 5 revolutions of the knob.The last ¿ to ¿ revolution of the knob could deliver a full 8cm of compression.
Where Was This Sold?
Distributed to China.
About Michigan Instruments, Inc.
Michigan Instruments, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report