Polaris Recalls Ranger Recreational Off-Highway Vehicles and ProXD, Gravely and Bobcat Utility Vehicles Due to Fire Hazard (Recall Alert)

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The drive belt can break during operation and damage the inner clutch cover assembly and fuel line, which can result in a fuel leak, posing a fire hazard.

Source: Recall List

KTM, Husqvarna and GASGAS Recall Closed Course Competition Motorcycles Due to Crash Hazard (Recall Alert)

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The drive chain can break, posing a crash hazard and/or property damage.

Source: Recall List

Real Water, Inc., Issues Precautionary Recall of All Sizes of Real Water Brand Drinking Water Due to a Possible Health Risk

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Real Water, Inc. of Mesa, AZ and Henderson, NV, has issued a voluntary recall of all sizes of its Real Water brand drinking water, because it may be linked to certain instances of non-viral hepatitis which were reported in or about November, 2020 in the Las Vegas, NV area.

Source: FDA Food Safety Recalls RSS Feed

Bit & Bet LLC Issues Voluntary Nationwide Recall of Thumbs Up 7 Blue 69K Due to Presence of Undeclared Sildenafil and Tadalafil

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Bit & Bet LLC is voluntarily recalling all lots of Thumbs Up 7 Blue 69K capsules to consumer level. FDA analysis has found the product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved produc

Source: Food and Drugs Administration--Recalls/Safety Alerts

Zydus Pharmaceuticals (USA) Inc. Issues Voluntary Nationwide Recall of Acyclovir Sodium Injection, 50 mg/mL Due to Crystallization

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Pennington, NJ, Zydus Pharmaceuticals (USA) Inc. is voluntarily recalling four lots of Acyclovir Sodium Injection, 50 mg/mL, 10 mL and 20 mL vials, to the Hospital/User level after receiving several complaints of crystallization in vials. Administration of crystalized Acyclovir Sodium Injection, 50

Source: Food and Drugs Administration--Recalls/Safety Alerts

Alembic Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Telmisartan Tablets, USP, 20 mg Due to Label Mix-Up

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Bridgewater, NJ, Alembic Pharmaceuticals, Inc is voluntarily recalling one lot of Telmisartan Tablets, USP, 20 mg, packaged in 30-count bottles, Lot No. 1905005661 to the consumer level. The product is being recalled due to a market complaint received which stated that one bottle labelled as 30-cou

Source: Food and Drugs Administration--Recalls/Safety Alerts

Flame King Recalls Hog 100-Pound Propane Cylinders Due to Fire Hazard

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The propane cylinders manufactured with a handle below the weld on the side could leak propane gas, posing a fire hazard.

Source: Recall List

Birdie Belay Devices Recalled Due to Risk of Injury; Made by Beal Sas

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The device user can be unable to lower the climber, posing a risk of injury to the climber.

Source: Recall List

GK Foods USA Announces Voluntary Recall of a Batch of La Fe Peppers and Onions

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GraceKennedy Foods (USA) LLC (GK Foods USA) has announced a voluntary recall of a batch of its La Fe Peppers and Onions, due to the probable presence of extraneous material. Derrick Reckord, President and CEO of GK Foods USA, owner of the La Fe brand, explained that the Voluntary Class 2 Recall has

Source: FDA Food Safety Recalls RSS Feed

Bobo’s Issues a Voluntarily Allergy Alert on Undeclared Peanuts in Product

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Bobo’s of Boulder, Colorado is issuing a voluntary recall of Bobo’s Maple Pecan Oat Bars because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products

Source: Food and Drugs Administration--Recalls/Safety Alerts