Michigan Instruments, Inc. Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000.
Brand
Michigan Instruments, Inc.
Lot Codes / Batch Numbers
All units sold in Japan (All serial numbers with 7- or 9- followed by 4 numbers, e.g. 7-xxxx or 9-xxxx).
Products Sold
All units sold in Japan (All serial numbers with 7- or 9- followed by 4 numbers; e.g. 7-xxxx or 9-xxxx).
Michigan Instruments, Inc. is recalling Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000. due to Failure to initiate compressions when turned on.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure to initiate compressions when turned on.
Recommended Action
Per FDA guidance
The Japanese distributor is instructed by letter dated 9/14/06 to drill a small hole in the male checked connector at the base of the column in order to allow rapid bleed off of the pressure and to give customers a revised operators manual.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026