95,102 total recalls in our database
Del Monte Fresh Produce N.A., Incorporated
Apples have the potential to be contaminated with Listeria monocytogenes.
Texas Star Nut and Food Co.
Product tested positive for Salmonella.
Krispy Kreme Doughnut
Finished product may contain foreign matter (glass).
Finished product may contain foreign matter (glass).
Valeant Pharmaceuticals North America
Failed Dissolution Specifications: Failed 24 month dissolution testing.
Vintage Pharmaceuticals LLC
Failed Stability Specifications: Out of Specification results obtained for preservative butylparaben.
GE Medical Systems
GE became aware of an issue with the table transfer release mechanism of the MR Surgical Suite Option. The issue may prevent patient transfer between the MR and surgical tables.
User settings were no longer on the monitor's memory after these systems were powered off and back on.
Inaccurate distance measurements with magnified projection X-ray images.
The packaging of 4.5 mm diameter MaxAn screws identifies/labels the screws as 4.0 mm diameter screws.
The recalled lot of custom paks are labeled as latex free and contain latex gloves rather than the specified non-latex gloves.
Philips Medical Systems (Cleveland)
The reason for this inspection is to determine if the Spindle Block Servo Controllers on the CT subsystem of potentially affected GEMINI PET/CT systems are susceptible to premature failure.
Interactive Motion Technologies
Unsupervised patient could potentially mis-use the device and remove or rotate a protective cover and expose a potential pinch hazard.
Once tested, it is required that the tourniquet be returned to its Ready position then placed in its packaging. Each tourniquet was tested for functionality, but in some cases, the tourniquet was not returned to its Ready position prior to packaging.
ELITech Clinical Systems reagents based on Trinder reaction used on the Selectra ProS and ProM systems are recalled due to potential drug interference. No complaints were received.
The firm determined that 25 lots had been manufactured with a minor surface defect occurring in the optical surface on each lens. Complaints of Halo or Poor Visual Acuity.
The locking pin on the RIO Base Array is damaged during assembly onto the RIO Base Array Connector.
Otto Bock Healthcare GmbH
A software issue can make the foot move into dorsiflexion, unnoticed by the user, who could fall. When sitting, the prosthetic foot can go into the Relief Function to move the footplate towards the ground. When operating machines with foot pedals (e.g. a car) the foot could get stuck under the foot pedal and block it or, with the foot on the pedal, it could cause unintended vehicle acceleration.
Potential failure mode related to the radial brake, where the detector was able to drift, led to a re-design of the brake redundancy circuit. The redesigned Brake Redundancy Circuit will force even a defective brake to engage in the unpowered state by applying a reverse charge to the brake and ensuring the brake has demagnetized.
ELITech clinical Systems reagents based on Trinder reaction used on the Eon 100 instrument system are recalled due to potential drug interference. No complaints were received.