Dated: NOV 13, 2018 Volvo Car USA LLC (Volvo) is recalling certain 2017-2019 Volvo XC90, S90, V60, V60 Cross Country, V90, XC40, XC60, and V90 Cross Country vehicles. The software installed in the Vehicle Connectivity M... … [Read more...]
Lumber Liquidators Recalls 5-Gallon Buckets Due to Drowning Hazard (Recall Alert)
Young children can fall into buckets and drown. The buckets do not have the required cautionary label warning of the drowning risk posed to young children. … [Read more...]
Öhlins Recalls Bicycle Forks Sold on Specialized Bicycles Due to Fall and Injury Hazards
The air cartridge can abruptly spring out of the stanchion tube, posing fall and injury risks to the rider. … [Read more...]
IKEA Recalls Dining Tables Due to Laceration Hazard
The table’s glass extension leaf can detach and fall unexpectedly, posing a laceration hazard. … [Read more...]
Cyberonics Vagus Nerve Stimulator Recalls
So far, there have been at least six recalls of model 106 generators used to power Cyberonics vagus nerve stimulator (VNS) therapy systems. The VNS therapy systems are implanted devices used to treat seizures and epilepsy. The U.S. Food and Drug Administration (FDA) has received more than 10,000 reports of injuries and death in people who have … [Read more...]
Pfizer Inc. Issues A Voluntary Nationwide Consumer Level Recall of Six Lots of Thermacare® Heatwraps Due to Leaking Wraps With The Potential For Skin Injuries
Pfizer Consumer Healthcare, a division of Pfizer Inc., is voluntarily recalling six lots of ThermaCare® HeatWrap product to the consumer level. Pfizer Consumer Healthcare initiated this recall because product from these lots has a potential to leak ingredients that are contained in the heat cell wrap. The use of a leaking/damaged heat cell wrap … [Read more...]
Ottogi America, Inc. Issues Allergy Alert on Undeclared Egg in Product
Ottogi America, Inc. of Gardena, California announced today it is recalling 1lb 5.16ounce of Jin Ramen Mild 5pk. (Best Before Aug. 19th 2019) and Jin Ramen Spicy 5pk. (Best Before Aug. 20th 2019) due to undeclared egg as an ingredient on the packages. People who have an allergy or severe sensitivity to eggs run the risk of serious or … [Read more...]
TRIPLE E ( 18V779000 )
Dated: NOV 02, 2018 Triple E Recreational Vehicles (Triple E) is recalling certain 2019 Triple E Unity motorhomes, models U24MB, U24CBB, U24TB, U24IX and U24FX. The driver-side front trans-mount leveling jack support br... … [Read more...]
SCION ( 18V776000 )
Dated: NOV 01, 2018 Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2004-2006 Toyota Scion xA vehicles. The air bag control module for the supplemental restraint system (SRS ECU) may experience an... … [Read more...]
FORD ( 18V782000 )
Dated: NOV 06, 2018 National Van Builders, Inc. (National Van) is recalling certain 2015-2018 Ford Transit vehicles equipped with Freedman GO-ES Foldaway Seats, part numbers 43705, 45467, 48923, and 75719. When the back... … [Read more...]
Chunwei, Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens and Monosodium Glutamate
WASHINGTON, Nov. 23, 2018 – Chunwei, Inc., a Huntington Park, Calif. establishment, is recalling approximately 65,023 pounds of various ready-to-eat and raw meat and poultry products because the products are misbranded and may contain soy, wheat, dairy, egg, and sesame, known allergens, as well as monosodium glutamate (MSG), which are not … [Read more...]
FDA Classifies Field Action Related to Fc 500™ And Epics® As Class 1 Recall Beckman Coulter Life Sciences Committed to Helping Customers Take Prompt, Appropriate Actions
Beckman Coulter Life Sciences today announced the previously communicated global voluntary recall launched in January 2018 related to the FC 500™ Series Flow Cytometers (FC 500), COULTER® EPICS® XL™ and COULTER® EPICS® XL-MCL™ Flow Cytometer with System II Software (together referred to as the EPICS) has been … [Read more...]
JEEP ( 18V786000 )
Dated: NOV 08, 2018 Chrysler (FCA US LLC) is recalling certain 2018 Jeep Wrangler four-door vehicles. The right rear passenger door latch may not be in the correct location, possibly preventing the door from latching pr... … [Read more...]
Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection, USP, 0.9% Due to Product Labeling Incorrectly Stating Stoppers Do Not Contain Latex
Fresenius Kabi USA is voluntarily recalling 163 lots of Sodium Chloride Injection, USP, 0.9%, 10 mL fill in a 10 mL vial and Sodium Chloride Injection, USP, 0.9%, 20 mL fill in a 20 mL vial to the user level. The product insert states that stoppers for both the 10mL and the 20mL vials do not contain natural rubber latex; the tray label for the two … [Read more...]
KEYSTONE ( 18V785000 )
Dated: NOV 06, 2018 Keystone RV Company (Keystone) is recalling certain 2019 Keystone Montana recreational trailers with the Legacy package. The fasteners that secure the disc brake assembly may fail. … [Read more...]
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