134 recalls tagged with “outdoor”.
iMirror Inc. recalls Electric Bug Zapper Racket, Fly Swatter and Mosquito Swatter sold on Amazon and at imirror.com on July 24, 2025. The recall cites a hazard where the rechargeable battery can catch fire with extended use. Consumers should stop using the products immediately and contact iMirror for a full refund.
Hyundai Motor America recalls 2025 IONIQ 5 vehicles due to a potentially loose bus bar in the high voltage battery system. The recall covers 2025 IONIQ 5 models. Hyundai says a short circuit could cause a fire. Owners should park outside away from structures until the remedy is complete and contact Hyundai at 1-855-371-9460. The recall number is 280.
Bestway, Intex and Polygroup recall 5 million above-ground pools taller than 48 inches after nine deaths. The recall covers pools whose model numbers are printed on the liner outside the pool. The hazard stems from a compression strap around the pool legs that can create a foothold for a child, enabling access to the water. Stop using the pools immediately and contact the respective brands for a维修
DJO Surgical recalled 927 ALTIVATE reverse wedge glenoid reamer heads distributed nationwide in the United States after concerns that the devices may kick or bind up during use. The issue involves model 804-06-311 and non-sterile stainless steel material. Healthcare providers and patients should stop using the device immediately and contact Encore Medical, LP for instructions.
Tractor Supply recalled three Traveller aluminum loading ramps on July 17, 2025 after determining a fall hazard. The ramps can bend or break under load. Stop using the recalled ramps and seek a full refund from Tractor Supply.
Creekliybear recalled its Pack and Play aftermarket mattresses sold on Amazon by Kbabyea on July 10, 2025. The mattresses exceed thickness standards and may not fit certain play yards, creating a suffocation entrapment risk. Parents should stop using the mattresses immediately and contact Kbabyea for a full refund.
SPPTTY recalled kids bicycles sold at Walmart after lead levels exceeded the federal lead content ban in multiple components and on the black paint used on pumps. The recall urges consumers to stop using the bicycles immediately. To receive a refund, dismantle the bicycles, photograph the setup, and email the photo to lishkjie@163.com; after destruction is verified, dispose of the bike.
Giant Bicycle recalls Momentum Vida E+ electric bicycles after a fork crash hazard. The recall affects bikes with specific serial numbers. Stop riding and contact Giant Bicycle for a fork replacement.
Boothwyn Pharmacy recalls 642 vials of semaglutide 2.5 mg/mL injection sold nationwide in the U.S. The recall cites subpotent drug with Class II designation. Consumers and healthcare providers should stop using the product immediately and contact Boothwyn Pharmacy for guidance.
Sedecal SA recalled 1 unit of the 40KW-FX.899 Mobile X-ray System distributed to CA, IL and NJ. The device is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could cause adverse effects. Stop using the device and contact Sedecal SA or a healthcare provider for instructions.
Sedecal recalled 1,198 MobileDiagnost wDR 2.2 mobile X-ray systems distributed in California, Illinois and New Jersey. The company reminded users the equipment is not water-resistant and must be cleaned strictly according to the manual. Improper cleaning could have consequences outlined by Sedecal. Health care providers should stop using the device immediately and follow recall instructions.
Sedecal SA recalled a single SM-40HF-B-D-C 40KW mobile X-ray unit distributed to California, Illinois and New Jersey. The device is not water-resistant and must be cleaned per the manual, with explicit warnings about improper cleaning. Stop using the device and contact Sedecal SA or your healthcare provider for instructions.
Chefs Warehouse recalled 15 lbs of diced cucumbers distributed to Maryland, Delaware and Virginia after Salmonella contamination was found. The recall is active as of May 20, 2025. Consumers should not consume the product and should contact Chefs Warehouse for refund or replacement.
Medtronic MiniMed recalled 1,440 Simplera Sensor units distributed outside the United States after a device cap label may not adhere, risking sterility. The defect could increase infection risk. Patients and healthcare providers should stop using the device and follow recall instructions provided by Medtronic MiniMed or their healthcare provider.