Harbor Freight Tools Recalls Chainsaws Due to Serious Injury Hazard Recall Date: May 14, 2018 Recall Number: 18-155 Name of Product: Portland, One Stop Gardens, and Chicago Electric 14 inch electric chainsaws Hazard: The power switch can malfunction and allow the chainsaw to continue
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Goodman Company Recalls Packaged Terminal Air Conditioners and Heat Pumps Due to Burn and Fire Hazards Recall Date: March 1, 2018 Recall Number: 18-113 Recall Summary Name of Product: Packaged Terminal Air Conditioners/Heat Pumps (PTACs) Hazard: The outdoor fan motors can overheat, posing
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Graco Recalls Highchairs Due to Fall Hazard; Sold Exclusively at Walmart Recall Date: March 1, 2018 Recall Number: 18-112 Recall Summary Name of Product: Graco Table2Table 6-in-1 Highchairs Hazard: The highchair’s rear legs can pivot out of position making the chair unstable and posing a
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Skip Hop Recalls Convertible High Chairs Due to Fall Hazard Recall Date: January 9, 2017 Recall Number: 18-078 Name of Product: Tuo Convertible High Chairs Hazard: The front legs on the highchair can detach from the seat, posing fall and injury hazards to children.
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Ravin Crossbows Recalls Arrow Nocks Due to Injury Hazard Recall Date: December 11, 2017 If the nock is not fully engaged with the bowstring, the crossbow can fail to discharge when the trigger is pulled and can result in the bow discharging
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Target Recalls Room Essentials 4-Drawer Dressers Due to Tip-Over and Entrapment Hazards The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in death or injuries to children. Units: About
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Our Ohio product liability attorneys are currently taking on Invokana claims related to amputations and ketoacidosis, which have been linked to the drug. Invokana (canagliflozin) is a prescription drug used to treat type-2 diabetes. It was approved by the FDA in 2013
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The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product(s): Datascope Corp./MAQUET Intra-Aortic Balloon Pump Model/Item Numbers: CS100i, CSO100, CS300 Lot Numbers: All Lots
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Liquid Drug Products Manufactured by PharmaTech and Distributed by Rugby Laboratories and Possibly Other Companies: FDA Advisory – Not to Use FDA is advising health care professionals and patients not to use any liquid product manufactured by PharmaTech LLC, Davie, Florida, due
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A child seated in the carrier can slip through the leg openings, posing a fall hazard to children. Consumers should immediately stop using the recalled carriers and contact Osprey for a free Seat Pad Insert for use along with the existing safety
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