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All product recalls associated with CAN-AM.
Total Recalls
1000
Past Year
899
Class I (Serious)
125
Most Recent
Jan 2026
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.
Bombardier Recreational Products, Inc. (BRP) is recalling certain 2025 Can-Am Canyon motorcycles. On these motorcycles, the drive belt lower idler support will fail and possibly cause a belt failure.
Lack of pasteurization and sanitation records
Lack of pasteurization and sanitation records
Lack of pasteurization and sanitation records
GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.
Mislabeling
GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.
Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.
Due to a component manufacturing issue, Automated External Defibrillator may not function properly (deliver shocks)
Potential for temporary loss of imaging (X-ray) functionality due to software issue.
Cannulated fenestrated polyaxial screws may be incorrectly labeled
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Potential to be contaminated with Listeria monocytogenes
Potential to be contaminated with Listeria monocytogenes
Potential to be contaminated with Listeria monocytogenes
Device does not comply with the labeling requirements of international standard IEC 60601-1.
Potential Listeria Monocytogenes Contamination
Potential Listeria Monocytogenes Contamination
Potential Listeria Monocytogenes Contamination
Potential Listeria Monocytogenes Contamination