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All product recalls associated with Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF).
Total Recalls
1000
Past Year
579
Class I (Serious)
91
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The back of some Medical Device Identification Cards provided to patients were printed with an erroneous statement stating the following: "This patient has a complete MR conditional system implanted."
The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger Kits) become unresponsive if the charging steps, indicated in the Recharger Patient User Guide, are not followed.
This recall involves the Elektron Power Handle BP-1, a portable power source for Elektron music synthesizers and music effects devices. The metal and plastic power handles measure about 11 inches wide, 3 inches deep and 1 inch high. They were sold with a connection cable and a screw. Recalled power handles have a serial number beginning with 4250A located on the inside edge of the battery compartment. UPC code 7350049242057 and Made in Sweden can be found on the back of the product packaging.