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All product recalls associated with Acumed LLC.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
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.
Product sterility may be compromised.
GE Healthcare has recently become aware of an error in the generator software on the Revolution XR/d configured with HP 8200 PC consoles that reports a mAs reading that is higher than is actually exposed to patients.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
Product sterility may be compromised.
A software error causes the wedge accessory calculation to be ignored in the radiotherapy treatment plan.
Skin irritation and burns with product usage
Skin irritation and burns with product usage
The firm's Altaire MR Scanner's Emergency Rundown Switch Unit (ERDU), that is used to shut down the device in an emergency, was found to be defective. An ERDU failure could delay or prevent patient access leading to possible patient death or serious injury.
The collimator could fall from the x-ray stand, due to loosening screws, and strike a patient or operator underneath.
Some jaws exhibited lack of ductility and could break if overloaded or used improperly by placing too much tissue in the bottom of the "v" of the jaw.