Reported May 16, 2018 · Terminated
Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370 Product Usage: The device is used to perform…
Michigan Instruments, Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Michigan Instruments, Inc. · 4717 Talon Ct SE · Grand Rapids, MI · 49512-5408
Is this the product you have?
Thumper Cardiopulmonary ResuscitatorModel 1007CCVCatalog No. 15370
- Product UsageThe 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
- Lot codes and dates
- CDNV - SN Installed In - Mfr Date
114 of 114 codes
5519CCV-218109/175518CCV-218209/175516CCV-218309/175517CCV-218409/175522CCV-219609/175531CCV-220012/175533CCV-220112/175538CCV-220212/175524CCV-220312/175523CCV-220412/175526CCV-220512/175528CCV-220612/175529CCV-220812/175535CCV-220912/175530CCV-221012/175534CCV-221112/175539CCV-221212/175520CCV-221312/175532CCV-221412/175525CCV-221512/17
- CDNV - SN Installed In - Mfr Date
- Amount recalled
- 38 devices
Why it was 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.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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