electrical hazard Recalls

1,120 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Pivotal Health Solutions Recalls 34 Quantum Q400 Heated Massage Tables for Overheating Risk (2025)

Pivotal Health Solutions is recalling 34 Quantum Q400 intersegmental heated massage tables sold nationwide in the United States, Canada and Japan. The recall cites heat-function components that can be damaged over time when pressed, risking overheating, smoldering and melting of the vinyl cushion. Clinicians and patients should stop using the device immediately and await manufacturer instructions.

Pivotal Health Solutions
The heat
Read more
Recalled Generic Magnetic Balls
HIGH
CPSC

Generic Magnetic Ball Sets Recalled for Magnet Ingestion Risk Sold on Amazon by Ritons (2025 recall)

Generic magnetic ball sets sold on Amazon by Ritons are recalled after a high-risk ingestion hazard was identified. The magnets, 3 mm in size and packed in sets of 1,000, can cause serious injury or death if swallowed. Consumers should stop using the recalled product immediately and contact Ritons for a refund with a prepaid return label.

Generic Magnetic Ball Sets
The recalled
Read more
Recalled Mom Genius retractable safety gate-black
HIGH
CPSC

Mom Genius Recalls Retractable Safety Gates for Entrapment Risk

Mom Genius recalled retractable safety gates due to entrapment risk that can cause serious injury or death. The recall covers gates with a retractable mesh screen in black and gray. The model is SH.20.006B02. Consumers should stop using the gate and seek a full refund.

Mom Genius
The recalled
Read more
Health & Personal Care
HIGH
FDA DEVICE

C-RAD POSITIONING AB Recalls Catalyst Device Over Treatment Risks

C-RAD POSITIONING AB recalled 189 Catalyst and Catalyst+ devices on October 9, 2025, due to issues with stereotactic radiosurgery (SRS) treatment. The defect may lead to incorrect patient positioning, potentially compromising treatment effectiveness. The recall affects devices distributed across 37 countries, including the United States.

C-RAD POSITIONING AB
Due to
Read more
Recalled YGJT Baby Lounger
HIGH
CPSC

YGJT Baby Loungers Recalled on SHEIN for Entrapment and Fall Risk (2025)

YGJT recalled baby loungers sold on SHEIN by YGJT Local Warehouse from June 2025 through August 2025 for $18-$21. The recall cites a safety violation that allows infants to be trapped or fall due to low sides, wide openings at the foot, and no stand. Consumers should stop using the loungers immediately and request a full refund by emailing YGJTrecall@outlook.com.

YGJT
The recalled
Read more
Food & Beverages
HIGH
FDA FOOD

Sno Pac Foods Frozen Organic Spinach Recall Affects 4,006 Cases (2025)

Sno Pac Foods recalled 4,006 cases of Frozen Organic Spinach sold under Sno Pac Frozen Vegetables and Maika'i Keep Frozen. The spinach may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact Sno Pac Foods for refund or replacement.

Sno Pac Foods
Organic Spinach
Read more
Recalled Evermore Surprise Egg – Yellow Wrap
HIGH
CPSC

In Motion Design Recalls Evermore Surprise Eggs for Lead Hazard

In Motion Design recalled Evermore Surprise Eggs due to lead content above federal limits. The recalled eggs were sold with yellow, pink or green wrap and include a gold egg containing seven toys, including a toy airplane. Consumers should stop using the product and return it for a full refund.

In Motion Design
The toy
Read more
Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella Controller Recall Aims to Address Cybersecurity Vulnerabilities Across 32 Product SK

Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.

Abiomed
Potential cybersecurity
Read more
Health & Personal Care
HIGH
FDA DEVICE

SHENZHEN ATOMSTACK TECHNOLOGIES Recalls Laser Products Over Safety Hazard

SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.

SHENZHEN ATOMSTACK TECHNOLOGIES
Lack of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland 718096 Zenition 50 Interventional X-Ray System Recalled in 2025

Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
Read more
Health & Personal Care
HIGH
FDA DRUG

Medline 222,800 Alcohol Prep Pads Recalled for Subpotent Drug (2025)

Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.

Medline Industries
Subpotent Drug
Read more
Health & Personal Care
HIGH
FDA DRUG

Acuity Specialty Products Hand Sanitizer Recalled for Methanol Risk Due to Unperformed Component-LOT

Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.

Acuity Specialty Products
cGMP deviations:
Read more
Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Cantaloupe Chunks Recall Expands for Listeria Contamination

Wholesale Produce Supply LLC recalled 307 cases of cantaloupe chunks sold under Fresh & Finest, Harvest Cuts and other labels. The recall targets a broad range of container sizes and UPCs in IA, IL, ND, NE and WI. The recall cites potential Listeria monocytogenes contamination and is classified as Class I.

Wholesale Produce Supply LLC
Potential Listeria
Read more
Health & Personal Care
HIGH
FDA DEVICE

Synthes 5.0mm IM Nail Locking Screws Recalled for Packaging Length Label Error (120 Units, 2025)

Synthes (USA) Products LLC recalled 120 low-profile locking screws for intramedullary nails used in the RFN-Advanced Retrograde Femoral Nailing System and the Tibial Nail Advanced System. The recall covers devices distributed worldwide through healthcare providers. The external packaging mislabels screw lengths: 42 mm screws are labeled 46 mm and 46 mm screws are labeled 42 mm. Hospitals and spine

Synthes
Although the
Read more
Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Cut Fresh Fruit Tray Recalled for Listeria Risk (2025)

Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Tray with Strawberries after potential Listeria monocytogenes contamination. The recall covers trays packed in Minneapolis, MN and distributed to Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The product should not be consumed and refunds or replacements are being offered. The recall is active as of the latest notice.

Wholesale Produce Supply LLC
Potential Listeria
Read more
Previous
12345...56
Next

Tag Statistics

Total Recalls
1,120

Related Tags

burn riskimmediate actionstop use immediatelyfda regulatedcpsc regulatedmandatory standard violationreplacement availablelithium batterybattery poweredfire hazardreturn for refundadult product
    electrical hazard Recalls | RecallRadar