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All product recalls associated with MRL, Inc., A Welch Allyn Company.
Total Recalls
1000
Past Year
620
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.
A faulty component has been identified which could result in an intermittent shock button (button #3) failure on the AED10 defibrillator.
If two of the four T-nuts that connect the transverse rail to the ceiling rail fail, the 'U' arm and transverse rails could fall and cause serious injury.
The guiding catheter provided with the SIS-10 biliary stent introduction system may be a 5 French instead of the required 6 French guiding catheter.