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.
64,666published records in database
4recall categories represented
May 2, 2018newest stored source record
Latest records
Latest recalls — page 1452
The newest recall records with useful source details are listed here.
Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages, with a green or orange Bayer logo located on the lower left corner of the front of the carton, because the…
Class IFDA: TerminatedBayer HealthCare Pharmaceuticals, Inc.
Pump was found to be constructed from crimp connectors that do not meet the fixation wiring requirements and can cause failure of the device to operate or electric shock or burn to the user.
Three lots of Human Fetal Hemoglobin FITC Conjugate are displaying high background and unusual bright staining in the controls and patient samples which could potentially lead to erroneous…
Class IIFDA: TerminatedLife Technologies Corporation
Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a report for a bone density exam may be sent to PACS with the incorrect patient information in the DICOM header.…
Class IIFDA: TerminatedGE Medical Systems Ultrasound & Primary Care…
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Following a period of inactivity, the mass storage device may cause the acquisition console to become unresponsive. This may prevent an acquisition from proceeding.
Class IIFDA: TerminatedPhilips Medical Systems (Cleveland) Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Control Console software has been updated to reduce the risk for collision when delivering automatically sequenced treatments with automatic movements of the gantry and/or the treatment…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
There is potential for a cart with disinfected goods to unload without the trolley being docked. Disinfected goods could end up falling to the floor causing risk to nearby users and damage…
These one-way valves may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient.
Class IIFDA: TerminatedTeleflex Medical Europe Ltd