Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Failed Tablet/Capsule Specifications: identification of low weight tablets during routine stability testing.
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Failed Content Uniformity Specifications: The product is out of specification for blend uniformity.
Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.
Microbial contamination
Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain undeclared sibutramine and phenolphthalein. Sibutramine is an appetite suppressant that was withdrawn from the…
Microbial contamination
Failed Content Uniformity Specifications: The product is out of specification for blend uniformity.
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Volvo Car USA LLC (Volvo) is recalling certain 2018-2019 XC60 and S90 vehicles. The driver and passenger front seat rail rear flange nuts may not have been installed during assembly.
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Atlas and 2020 Passat vehicles. An incorrect driver and/or front passenger side impact air bag may have been…
Braun Corporation (Braun) is recalling certain 2018-2019 Honda Odyessy vehicles modified to be equipped with an in-floor wheelchair ramp conversion. The rear wheel speed sensor harnesses…
Chrysler (FCA US LLC) is recalling certain 2019 Jeep Wrangler and 2019 Ram 1500 vehicles. These vehicles have improperly machined steering column stub shafts that may break, possibly…
Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced expiration date from 24 months to 13 months.
The swivel arm holding the monitors may become dislodged from the carrying arm.
The swivel arm holding the monitors may become dislodged from the carrying arm.
The firm is recalling their Delta family of patient monitors software due to cybersecurity vulnerabilities, which may cause the device to reboot, lose functionality, and/or lose…
Browse recent months with enough recall history for useful comparison.
