37 recalls tagged with “outdoor”.
Yeeluzan recalled two-pack pool drain covers sold on Amazon. The covers measure 8.7 inches in diameter and weigh 1.7 pounds. They are white ABS plastic and packaged as two-packs. Pool owners should stop using these recalled covers and request a full refund.
Wybotics is recalling specific Osprey 700 Max and S1 robotic pool vacuums sold through retailers after reports that the lithium-ion battery can overheat, creating a burn and fire hazard. The recall covers Osprey 700 Max models WY3312MAX and WY100MAX and S1 WY200, with serial numbers WY100M230117XXXX, WY100M230127XXXX, WY100M230130XXXX, WY100M230318XXXX, WY200-230328XXXX and W200**230330XXXX. The U
Shenzhen Shijingjie Network Technology recalled two models of male-to-male extension cords sold at Walmart after safety concerns. The cords pose a risk of electrocution and carbon monoxide poisoning when used for backfeeding from a generator into a home. Consumers should stop using the recalled cords immediately and contact the company for a full refund.
BISSELL recalled more than 1 million Steam Shot OmniReach handheld steam cleaners with attachments, sold nationwide through retailers. The attachments can detach and expel hot water or steam, posing a serious burn hazard. Stop using the attachments immediately and contact BISSELL to receive free replacement attachments.
Muscccm pool drain covers sold on Amazon by SZ Hengxun are being recalled. The covers measure 7 in long by 6.5 in wide by 1.8 in tall and weigh 11.7 oz. They are white ABS plastic with “Muscccm” printed on the packaging. The recall cites entrapment and drowning hazards and VGBA violations. Pool owners should stop using the recalled covers and seek a full refund.
SCUBAPRO recalled Monorail Weight Pockets for BCDs sold by retailers worldwide on 2026-04-09 after safety reviews identified a serious entrapment risk. The recall notes a potential for entrapment and drowning and cites missing warning labels. Consumers should stop using the recalled bed rails and contact SCUBAPRO for a full refund.
Seasonal Specialties recalled the Member's Mark 7-foot Pre-Lit Twinkling Buck sold online at Sam's Club after a burn hazard was identified. The recall centers on wiring that can overheat if connected incorrectly. Consumers should stop using the Buck immediately and contact Seasonal Specialties for a full refund or a repair kit.
Head USA recalls ski boots with fluorescent yellow components from 2016–2022 model years. The recall covers boots and inserts with six-digit article codes. Consumers should stop using recalled boots immediately and contact Head for a free replacement or sole-insert option.
Amazon recalled the Amazon Basics Camping Folding Pocket Knife sold by Amazon after a laceration hazard was identified. The knife has a 3.5-inch blade. The folding mechanism can fail to remain securely closed, posing a risk of serious cuts.
Specialized recalled all Turbo Como SL electric bicycles sold online at specialized.com and through Authorized Specialized Retailers. A fatigue crack in the fork steerer tube can cause progressive fork failure and a fall. Owners should stop riding immediately and arrange a free fork replacement at an Authorized Dealer; replacement parts are expected in Spring 2026.
Aisstxoer adult bicycle helmets sold on Amazon by YXTDZ Store are being recalled. The helmets fail to meet mandatory safety standards for impact attenuation and stability, creating a serious head-injury risk. Stop using the recalled helmet now and contact YXTDZ Store for a full refund; destroy the helmet and email a photo to yxtdzamz@126.com.
LFTE USA recalled Playground Swing Set Seats on March 12, 2026. The swing seats pose a fall hazard due to potential rivet failure. The recall affects model number 999604 with the code 'LF-65708' marked on the seat pad.
Rising Pharmaceuticals recalls 1,200 Temozolomide 5 mg capsules nationwide after a stability test found out-of-spec impurities. The drug is Rx-only, with NDC 16571-816-51 and lot 1TM0524003A. Stop using immediately and contact a healthcare provider for guidance.
Philips Medical Systems Nederland B.V. recalled 5,084 ALLURA Xper FD20 imaging systems sold nationwide and internationally after finding that the wired foot switch may fail to initiate X-ray imaging or perform intermittently. The defect can delay or interrupt imaging during patient care. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.
Civco Medical Instruments Co. recalled 21 eTRAX Needle Sensors for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The devices have an inspection and programming error that can cause the needle tip position to be misidentified on the user interface. Clinicians should stop using the devices immediately and follow recall instructions from Civco.
Olympus recalled 32 SOLTIVE Pro SuperPulsed Laser System units distributed worldwide after a defect in the 24V power supply may render the device inoperable. The defect can cause smoke or a burning smell, but the issue is contained within the laser console enclosure and self-extinguishing. Stop using the device and follow the manufacturer’s recall instructions.
Nilotinib capsules manufactured for Cipla USA are recalled nationwide after stability testing showed out-of-spec results. The failure involves description and appearance by visual inspection at six months of long-term stability. Patients and healthcare providers should stop using the product immediately and contact Cipla USA for guidance.
Navajo Manufacturing recalled 28,457 Handy Solutions Neck & Shoulders Heating Pads sold nationwide through Multiple Retailers. The defect allows overheating if the pad is folded or placed under the body, and the high limit device may fail to shut off. Stop use and contact Navajo Manufacturing for instructions.
Olympus Corporation of the Americas is recalling 2,929 units of the OER-Elite Endoscope Reprocessor in the United States. The MAJ-1443 and MAJ-1444 modules are no longer reprocessing compatible with the OER-Pro and OER-Elite systems. Hospitals and healthcare providers should stop using the affected devices immediately and follow the recall instructions issued by Olympus.
Orthalign recalled 7 pegged drill plates used with the Lantern Knee System due to out-of-spec manufacturing that can cause bone cuts up to 2.8448 mm. The devices were distributed in Utah and across the United States. Healthcare providers and patients should stop using the device immediately and await recall instructions by letter.