Michigan Instruments recalls Thumper Cardiopulmonary Resuscitator Model 1007CCV due to potential failure in delivering consistent chest compression depth during CPR. Affected units sold from 2017-2018.
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.
Michigan Instruments is recalling Thumper Cardiopulmonary Resuscitators Model 1007CCV because the chest depth needle valve may not deliver proper compression depth during the first 5 knob turns. This could lead to inadequate CPR performance in emergencies, potentially harming patients needing resuscitation.
The chest depth needle valve (CDNV) may not deliver any compression depth to the piston during the first 5 revolutions of the knob. After these initial turns, the device might deliver full 8cm compression in the last half revolution, but this inconsistency could result in ineffective CPR during critical emergencies.
Healthcare professionals and emergency responders who use the Thumper device for CPR on adult patients. Those with the specific model and serial numbers listed in the recall are most at risk.
Check for the model number 1007CCV and catalog number 15370. Affected units were manufactured with specific serial numbers (CCV-2181 to CCV-2233) between September 2017 and January 2018.
Verify the model number is 1007CCV and catalog number 15370.
Rotate the knob 5 times to ensure consistent chest compression depth is delivered.
The chest depth needle valve may not deliver proper compression depth during the first 5 revolutions of the knob, potentially leading to ineffective CPR.
Model 1007CCV with catalog number 15370, manufactured with specific serial numbers from September 2017 to January 2018.
No, but you should test the compression depth by rotating the knob 5 times to ensure it delivers consistent compression.
We’ve drafted a message you can send Michigan Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-1632-2018 — Michigan Instruments Michigan Instruments Hello, I own a Michigan Instruments that is covered by recall Z-1632-2018 from Michigan Instruments. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
