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 Resuscitator
    • Model 1007CCV
    • Catalog 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

    • 5519
    • CCV-2181
    • 09/17
    • 5518
    • CCV-2182
    • 09/17
    • 5516
    • CCV-2183
    • 09/17
    • 5517
    • CCV-2184
    • 09/17
    • 5522
    • CCV-2196
    • 09/17
    • 5531
    • CCV-2200
    • 12/17
    • 5533
    • CCV-2201
    • 12/17
    • 5538
    • CCV-2202
    • 12/17
    • 5524
    • CCV-2203
    • 12/17
    • 5523
    • CCV-2204
    • 12/17
    • 5526
    • CCV-2205
    • 12/17
    • 5528
    • CCV-2206
    • 12/17
    • 5529
    • CCV-2208
    • 12/17
    • 5535
    • CCV-2209
    • 12/17
    • 5530
    • CCV-2210
    • 12/17
    • 5534
    • CCV-2211
    • 12/17
    • 5539
    • CCV-2212
    • 12/17
    • 5520
    • CCV-2213
    • 12/17
    • 5532
    • CCV-2214
    • 12/17
    • 5525
    • CCV-2215
    • 12/17
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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 3, 2019 · Data as of Sep 19, 5:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.