back to school Recalls

54 recalls tagged with “back to school”.

Recalled Shenzhen Shijingjie Network Technology Extension Cord – blue
HIGH
CPSC

Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled in 2026 Walmart Recall

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.

Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords
The recalled
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Food & Beverages
HIGH
FDA FOOD

Pure Vitamins and Natural Supplements Boner Bears Honey Recall for Undeclared Sildenafil and Tadalaf

FDA analysis found undeclared sildenafil and tadalafil in Boner Bears Honey 100% Wildflower Honey. The recall covers 15-pouch boxes manufactured in Florida with distribution in New Jersey. Consumers should stop using the product and seek refund or replacement from Pure Vitamins and Natural Supplements.

Pure Vitamins and Natural Supplements
FDA analysis
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Vehicles & Parts
HIGH
NHTSA

Toyota recalls 2022-2025 Tundra and Tundra Hybrid over reverse light moisture risk

Toyota recalls 2022-2025 Tundra and Tundra Hybrid vehicles because moisture in the reverse light assemblies can cause light failure. Dealers will replace both reverse light assemblies and repair wire harnesses. Owner letters were mailed September 11, 2025. Contact Toyota at 1-800-331-4331 for recall 24TB06 and 24TA06.

Toyota Motor Engineering & Manufacturing
Reverse light
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Health & Personal Care
HIGH
FDA DEVICE

Civco Medical Instruments Recalls 21 eTRAX Needle Sensors for Aurora Trackers (2026)

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.

Civco Medical Instruments Co.
There was
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Vehicles & Parts
HIGH
NHTSA

AUDI Q3 Recall 2025 for Rear-Visibility Camera Software Update

Audi Q3 vehicles are recalled in 2025 for a rearview camera software issue. The camera control unit may fail at startup, causing the rear view to not display. Audi and Volkswagen owners should contact their respective dealers for details and to verify if their vehicle is affected.

AUDI
A rearview
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Recalled Vivohome Adult Portable Bed Rail - Model VH1316-WC
HIGH
CPSC

Vivohome Recalls Adult Portable Bed Rails for Entrapment Hazard in 2025

Vivohome recalled adult portable bed rails due to a risk of entrapment and asphyxiation. The recall covers models VH1316-WC and VH1316-WH. The rails measure about 36.6 inches long, 16.1 inches wide and 15.7 inches high and have a wooden or metallic top bar with a red release button that can collapse. Stop using the recalled rails and contact Vivohome for a full refund.

Vivohome
The recalled
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Recalled Vevor Baby Swing in White/Gray with White Base and Mosquito Net, Model Number BB501
HIGH
CPSC

Sanven Technology Recalls 3 Vevor Baby Swing Models for Suffocation Risk (2025)

Sanven Technology recalls 3 Vevor Baby Swing models on 2025-11-06 for a suffocation risk linked to an incline greater than 10 degrees. The swings carry the VEVOR trademark and are labeled as Multi-Function Electric Swing with model numbers BB501K, BB702A, and BB005. Consumers should stop using the swings immediately and contact Sanven Technology for a full refund.

Sanven Technology
The swings
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Recalled Halloween-themed Skeleton Wax Candle
HIGH
CPSC

Kroger Recalls Halloween Skeleton Wax Candles for Fire Hazard (2025)

The Kroger Co. recalls Halloween-themed Skeleton Wax Candles sold at Kroger stores due to a fire hazard. The candle contains flammable ornaments that create a burn risk. Consumers should stop using the candle immediately and return it to any Kroger store for a full refund.

Kroger
The candle
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical 490202 Extension Set Recall: 13,600 Units Over Backflow Risk (2025)

B Braun Medical Inc recalled 13,600 extension set units used with Infusomat Space and related pumps sold through multiple healthcare distributors worldwide. The recall cites a backflow risk from secondary piggyback containers into primary IV containers and an inability to prime due to occlusion. Healthcare providers and facilities should stop using the device immediately and follow manufacturer-re

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Sets Recalled for Backflow and Occlusion Risk (490549, 490565)

B. Braun Medical Inc. is recalling 65,232 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump worldwide. The devices pose a risk of backflow from secondary piggyback IV containers into primary IV containers and may fail to prime due to occlusion. Hospitals and healthcare providers should stop using the affected sets immediately and follow the maker

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Extension Set Recalled for 1,200 Units Over Backflow and Occlusion Risk (2025 Recall

B Braun Medical recalled 1,200 extension sets used with Infusomat Space large-volume pumps distributed worldwide to hospitals and clinics. The recall cites potential backflow from secondary IV containers into primary containers and an inability to prime (occlusion). Healthcare facilities should stop using the devices immediately and follow the recall instructions issued by the manufacturer.

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 32,500 Caresite Extension Sets for IV Pumps (2025)

B. Braun Medical recalled 32,500 Caresite Extension Sets used with Infusomat Space, Outlook, and Vista Basic IV pumps worldwide. The devices pose a backflow and occlusion risk in the primary IV line. Hospitals and healthcare providers should stop using the device immediately and follow the recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Anesthesia IV Set Recalled for Backflow Risk (10,536 Units) 2025

B. Braun Medical recalled 10,536 Anesthesia IV Sets sold through multiple retailers worldwide after a potential backflow from piggyback to primary IV lines and occlusion. The devices are used with Infusomat Space Large Volume Pumps, Outlook Pumps, and Vista Basic Pumps. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall for 29,900 Units Over Backflow and Occlusion Risk (202

B. Braun Medical recalled 29,900 IV administration sets distributed worldwide through medical distributors. The recall is linked to backflow from secondary to primary IV containers and an inability to prime. Healthcare providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Extension Set Recall 2,100 Units Over Backflow Risk (2025)

B. Braun Medical Inc. recalled 2,100 IV Extension Sets used with Infusomat Space, Outlook and Vista Basic pumps sold worldwide to healthcare facilities. The extension set presents a backflow risk from secondary to primary IV containers and can hinder priming. Hospitals and clinicians should stop using the device immediately and follow the recall instructions provided by the manufacturer.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for 126,050 Units Over Backflow Risk (2025)

B. Braun Medical recalled 126,050 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The recall cites potential backflow from secondary to primary IV containers and an inability to prime. Health care providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Inc. Recalls 28,344 IV Administration Sets Linked to Backflow and Occlusion Risks (Z

B Braun Medical Inc. recalls 28,344 IV administration sets used with several BBMI infusion pumps after reports of backflow and occlusion risks. The recall covers a catalog number 470179 device distributed worldwide including the U.S., Canada, Germany, Guatemala and Singapore. The issue involves potential backflow from secondary IV containers into primary containers and the inability to prime the管.

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall 23,160 Units for Backflow Risk in 2025

BBraun Medical recalled 23,160 IV administration sets distributed worldwide, including the US and Canada, after reports of backflow and occlusion risk. The recall involves catalog number 490487 and UDIs 04046955086856 and 04046955086849. Stop using the product immediately and follow manufacturer instructions for recall procedures.

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalled 19,320 Anesthesia IV Sets for Backflow Risk (2025)

B. Braun Medical Inc. recalled 19,320 Anesthesia IV Sets used with Infusomat Space Large Volume Pumps and related BBMI devices sold worldwide through healthcare facilities. The devices pose a backflow risk from secondary piggyback IV containers into the primary IV container and cannot be primed. Healthcare facilities and patients should stop using the device immediately and follow the manufacturer

B. Braun Medical
Potential for
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Tag Statistics

Total Recalls
54

Related Tags

electrical hazardimmediate actionstop use immediatelyreturn for refundpoisoning risklithium batteryworkplacegarageoutdoorplasticmetaltoddler product