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All product recalls associated with U & I America.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
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.
Reports of hex driver tips breaking off or becoming worn or stripped.
System failed to meet the mA's accuracy specfications at low mA's values
Catheter distal tip may separate
System failed to meet the mA's accuracy specfications at low mA's values
Reports of hex driver tips breaking off or becoming worn or stripped.
adjustment screw may break due to material fatigue
The device is not stable throughout its labeled expiration date.
adjustment screw may break due to material fatigue
This device is not approved for sale in the US.
Increased numbers of lens tears during placement of lens into eye.
mislabeled - product actually Single Valve
Potential loose header (end cap) on hollow fiber dialyzers.
Restoration T3 Revision Hip System distal stem has demonstrated fractures.
Potential loose header (end cap) on hollow fiber dialyzers.
Users may be pinched in the siderail assembly when raising or lowering the siderail.
The firm is withdrawing claims that pleural, pericardial, ascitic and cerebrospinal fluids are appropriate sample types for use on these instruments.
The firm is withdrawing claims that pleural, pericardial, ascitic and cerebrospinal fluids are appropriate sample types for use on these instruments.
Tubes are brittle and break during centerfuging specimens.
The firm is withdrawing claims that pleural, pericardial, ascitic and cerebrospinal fluids are appropriate sample types for use on these instruments.
The firm is withdrawing claims that pleural, pericardial, ascitic and cerebrospinal fluids are appropriate sample types for use on these instruments.