Recall Z-0178-2007 ยท DRM Compressor, Cardiac, External
Michigan Instruments, Inc.
Michigan Instruments Thumper Mechanical CPR Device; Model 1007, Part number 15000.
| Date | Nov 14, 2006 (initiated Sep 14, 2006) |
| Status | Terminated |
| Reason | Failure to initiate compressions when turned on. |
| Root cause | Other |
| Action | 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. |
| Quantity | 639 |
| Distribution | Japan. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K972525 | THUMPER Michigan Instruments, Inc., Oct 2, 1997 |