Complete FDA and NHTSA recall records dated in 2019, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2012-2020 Volkswagen Passat and 2018-2019 Atlas vehicles. The blocking cap disabling the adjustment of the headlight's…
Honda (American Honda Motor Co.) is recalling certain 2019 CR-V vehicles. The metal core of the steering wheel may have burrs which can damage the harnesses routed within, potentially…
There is a potential of fracture, bending or shearing of the driver.
There is no warning in the Elekta Unity manual for the administration of gadolinium-based or other contrast agents for imaging or image guidance purposes has not been validated.
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
There were multiple issues identified in the system software which required an update.
Continuous operation at very high tube output may result in increased wear of the radiation emitting components. This may occur when tube voltages of 125 kV are used for a long period, e.g.…
There were multiple issues identified in the system software which required an update.
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
The application may be closed by the operating system without alerting the user the app is no longer running or communicating with the transmitter resulting in the user not receiving alerts…
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
There is a potential to generate falsely elevated serum or plasma chloride results when using the product.
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
There were multiple issues identified in the system software which required an update.
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
If cables are improperly connected, current may reach high charge density, causing tissue harm.
Luminometer Malfunction May Cause Inability to Process MicroWell Assays on VITROS Systems
Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
Voids in the seal or a partial seal results in an open channel and may compromise the sterility of the product
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
