95,114 total recalls in our database
Delta Med SpA
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Olympus Corporation of the Americas
Thermal injury following dusting and fragmenting treatment of ureteral stones when user exceeded the 20W standard presets
Howmedica Osteonics
The internal profile of the Triathlon Prim (Baseplate) is potentially oversized; there may be a witness mark (taper) at the bottom of the internal profile of the baseplate, which prevents the insert from locking on the baseplate.
Philips Ultrasound
Ultrasound system control panel arm swivel lock could fail, which could cause the control panel and monitor to swivel freely while a user is positioning the monitor, or transporting/moving the system, which could lead to patient or user musculoskeletal injury.
Philips North America
When setting patient weight unit preferences to pounds, SynchRight P3T (Personalized Patient Protocol) software will result in increased contrast volume, resulting in increased contrast volume recommended for the patient.
Angioplasty system has a manufacturing issue that has the potential to result in difficulty deflating the outer balloon, which may result in increased risk of access site complications.
Boston Scientific
Potential for leaks and loosening at the patient catheter connection
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med SpA
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med SpA
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Mislabeled: Labeled on the package as 60mm contains 45mm devices
Units are displaying output readings that differ from the measurements taken using a Gas Analyzer. When the display is reading a target setting of 5%, an external meter is reading between 3% and 12% and the Incubator does not alarm. May result in loss of embryo during storage.
Two software issues have been identified related to pressure increase in the device: The first issue is described as "Infant/Pediatric EFS Calibration Pressure Increase" and the second issue is described as "Pressure Drift (Continuous Usage).
EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Unknown Manufacturer
The lithium-ion GLW battery packs in the self-balancing scooters/hoverboards can overheat, posing a risk of the products smoking, catching fire and/or exploding.
Unknown Manufacturer
The octopus and elephant puzzle pieces can break, posing a choking hazard to young children.
Qingdao Ruizexin Electronic Technology Co. Ltd., of China
The bath seats fail to meet the federal safety standard for infant bath seats, including requirements for stability and leg openings, and can tip over while in use, posing a drowning hazard to babies.
Deere & Company, of Moline, Ill.
Rear wheel spacer bolts that were torqued improperly during manufacturing can cause the wheel to fall off during use. This can result in the tractor overturning, posing an injury hazard to the operator.
5000 Years Foods
potential to be contaminated with Listeria monocytogenes
Firm notified by customers that product labeled as Dark Chocolate Malt Balls had Dark Chocolate Peanut Butter malt balls inside - undeclared peanuts.