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All product recalls associated with C.R. Bard Inc.
Total Recalls
1000
Past Year
432
Class I (Serious)
138
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.
There is potential for packaging defects that may impact the sterile barrier.
There is potential for packaging defects that may impact the sterile barrier.
There is potential for packaging defects that may impact the sterile barrier.
The EXAM acquisition workflow could occasionally freeze after canceling the PET scan.
The EXAM acquisition workflow could occasionally freeze after canceling the PET scan.
Sling loop straps on device pose a trip hazard.
Lack of sterility assurance
Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials will cause the instrument to generate a warning that calibrators are incorrectly loaded and calibration will not be completed successfully.
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Failed Stability Specification; Out of specification for Osmolarity
Lack of CGMP: This recall is being carried out due to potential for carry over of Senna Syrup.
Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.
Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.
Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.
Test strip vials may open while inside sealed cartons during shipment. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences.
Fish not declared as an allergen
Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2019 G550 vehicles. The fuel tank may not have been welded properly during manufacturing, which could result in a fuel leak.
Complaints have been received for performance issues related to high background and staining. this issues is related to a manufacturing process error that can potentially cause a false positive staining due to contamination with another antibody.
Device failed to function as intended and/or failed to conform to their design specifications.