All Recalls

95,018 total recalls in our database

๐Ÿฅ Medical Devices Class I - Dangerous

Four potential software issues with Artis pheno and Artis icono systems with software VE20C: 1. Updated calibration data not saved with measurement after scene+/-; 2. No x-ray possible, system shutdown/restart might be required during intervention; 3. Corrupted Image during Roadmap; 4. Unintended shutdown of Imaging System with UPS (Uninterruptable Power Supply) option

Oct 12, 2021 Diagnostic Equipment Nationwide View Details โ†’

Risk of misidentification or delayed results with the absence of identification due to thermoforming defect.

Dec 20, 2021 Diagnostic Equipment View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

The firm is reinforcing the IFU instructions: "Do not use if the package is damaged." If upon inspection of the packaging, any damage is observed, including pinholes or tears in the pouch, the product should not be used.

Dec 22, 2021 Surgical Instruments View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.

Nov 4, 2021 Other Medical Devices Nationwide View Details โ†’

Philips has identified a specific lot of non-conforming material manufactured by one of its suppliers. A Philips supplier incorrectly used polyester-based polyurethane (PE-PUR) sound abatement foam, a non-conforming material in the devices and repair kits. PE-PUR foam may degrade into particles which may enter the device s air pathway and be ingested or inhaled by the user. The foam degradation may be exacerbated by use of unapproved cleaning methods such as unapproved ozone cleaners, and the PE-PUR foam may off-gas certain chemicals during initial use of the device.

Dec 22, 2021 Patient Monitors View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Incomplete sealing of blood collection device unit packages may produce a breach in the sterile barrier enclosing the product. This could lead to microbial contamination of the device prior to use. The health effects range from no clinical effect up to bloodstream infection.

Nov 10, 2021 Infusion Pumps Nationwide View Details โ†’

MAGEC 1 System

NuVasive Specialized Orthopedics

๐Ÿฅ Medical Devices Class I - Dangerous

Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.

Jun 25, 2019 Other Medical Devices View Details โ†’

Children's Robes

Unknown Manufacturer

๐Ÿ  Consumer Products Class II - Moderate

The children's robes fail to meet the federal flammability standards for children's sleepwear, posing a risk of burn injuries to children.

Feb 2, 2022 Children's Products Nationwide View Details โ†’
๐Ÿ  Consumer Products Class II - Moderate

The hinge-closers can malfunction and not fully self-close gates when installed. This can lead to unintended access to pools and other areas, posing injury and drowning hazards to young children.

Feb 2, 2022 Other Consumer Products Nationwide View Details โ†’
๐Ÿ  Consumer Products Class I - Dangerous

The ATVs fail to comply with the requirements of the federal mandatory ATV safety standard. The youth ATVs fail to meet the maximum speed limitations for vehicles intended for children ages 6, 10 and 12 years and older, or for teenagers, depending on the model. Additionally, for certain ATVs, the parking brakes do not prevent the movement of the vehicle. ATVs that fail to meet the mandatory safety requirements pose a risk of serious injury or death.

Feb 2, 2022 Children's Products Nationwide View Details โ†’