cpsc regulated Recalls

1,716 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical BAT Coverage Recall 1,489 Units Worldwide in 2026

Burlington Medical recalled 1,489 BAT Coverage units worldwide on 2026-02-11 after a design-related issue was identified. The recall targets attenuation material used in the device. The defect could affect the lifespan of the shielding. Healthcare providers and patients should stop using the device and follow manufacturer instructions. The recall is active as of 2026-04-08.

Burlington Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Leg Wraps Recall: 103 Units Worldwide in 2026

Burlington Medical, LLC recalled 103 leg wrap devices distributed worldwide through multiple retailers. The recall cites attenuation degradation over time that could shorten the devices' lifespan. Healthcare providers and patients should stop using them immediately and follow the manufacturer's recall instructions.

Burlington Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Demi Half Aprons Recalled for Attenuation Degradation Risk (2026)

Burlington Medical recalled 29 Demi Half Aprons distributed worldwide after finding attenuation material may degrade over time. The degradation shortens the protective lifespan. Healthcare facilities should stop using the aprons immediately and follow the manufacturer’s recall instructions.

Burlington Medical
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Thyroid Shield Recall 2026 Affects 41,962 Units Worldwide

Burlington Medical recalled 41,962 Thyroid Shield units worldwide after identifying attenuation degradation that could shorten the device’s lifespan. The attenuation material may degrade over time, reducing shielding effectiveness. Patients and healthcare providers should stop using the device immediately and follow the recall instructions in the manufacturer notice.

Burlington Medical
Potential for
Read more
Food & Beverages
HIGH
FDA FOOD

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Juniper Granola recalled 1,800 Junebar Chocolate Cherry All Natural Snack Bars sold in New York after undeclared milk and soy were found. The bars carry Lot L1300 and variants L1300A and L1300B. They were produced in a facility that also processes gluten, peanuts, and sesame. Consumers should not eat these bars and should contact Juniper Granola for refunds or replacements.

Juniper Granola
Products contain
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Puracol Collagen Wound Dressings Recalled for Elevated Endotoxin Levels (2026)

Medline recalled 108,971 units of Puracol MSC8522 and Puracol Plus MSC8622EP collagen wound dressings nationwide in the United States, with distribution to Mexico and Panama. Elevated endotoxin levels were identified in affected lots. Stop using the dressings and follow recall instructions provided by Medline or your healthcare provider.

Medline Industries, LP
Elevated endotoxin
Read more
Health & Personal Care
HIGH
FDA DEVICE

Orthalign Lantern Knee Drill Plate Recalled for Bone-Cut Risk (2026)

Orthalign recalled 7 drill plates used with its Lantern Knee System distributed nationwide, including Utah. The parts were manufactured out of specification and can cause a bone cut up to 0.008 inch (2.8448 mm). Healthcare providers were notified by letter and instructions to stop using the devices.

Orthalign
Drill plates
Read more
Health & Personal Care
HIGH
FDA DEVICE

Orthalign Drill Plate Recall 2026 for 7 Units Over Bone-Cut Risk

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.

Orthalign
Drill plates
Read more
Health & Personal Care
HIGH
FDA DRUG

LEO Pharma Recalls Adbry Injection Over Sterility Concerns

LEO Pharma Inc. recalled 11,407 units of Adbry injection on February 10, 2026. The recall stems from a lack of assurance of sterility due to particulate matter identified as wool fiber. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

ADBRY
Lack of
Read more
Food & Beverages
HIGH
FDA FOOD

SLADE GORTON Recalls Salmon Over Listeria Contamination

SLADE GORTON & CO. recalled 190 cases of Wellsley Farms Atlantic Salmon on February 10, 2026. The product may contain Listeria monocytogenes, a serious health risk. Consumers should not consume this product and seek a refund or replacement.

SLADE GORTON & CO.
Contaminated with
Read more
Health & Personal Care
HIGH
FDA DEVICE

Reflexion Medical Recalls 12 RefleXion X1 Radiotherapy Systems for Software Defect (2026)

Reflexion Medical recalled 12 RefleXion X1 Radiotherapy System RXM1000 units sold to hospitals and healthcare providers in the United States after a software defect could cause a 5mm or greater misalignment and underdose. The defect occurs during angular roll corrections followed by a repeat localization, and the roll corrections from the initial localization are not carried through to treatment.

Reflexion Medical
Due to
Read more
Recalled Aroeve MK04 Air Purifier in white
HIGH
CPSC

Airova Recalls Aroeve Air Purifiers Due to Fire Hazards

Airova recalled Aroeve air purifiers on February 9, 2026, due to fire and burn hazards. The recall affects model MK04 with serial numbers starting with 'BN' manufactured before July 2025. Consumers should stop using these air purifiers immediately and seek replacements.

Airova
The air
Read more
Food & Beverages
HIGH
FDA FOOD

H & N Group Recalls Frozen Shrimp Over Cesium-137 Risk

H & N Group recalled 378 cases of frozen cooked shrimp on February 9, 2026. The product may be contaminated with Cesium-137 due to insanitary manufacturing conditions. Consumers should not consume the shrimp and seek refunds.

H & N Group
Product manufactured
Read more
Food & Beverages
HIGH
FDA FOOD

Valley Springs Distilled Water Recalled Over Insanitary Conditions

Valley Springs Artesian Gold recalled 263,440 gallons of distilled water on February 6, 2026. The water was bottled under insanitary conditions, posing a health risk. Consumers in Illinois and Wisconsin should not consume the affected products.

Valley Springs Artesian Gold
Water was
Read more
Food & Beverages
HIGH
FDA FOOD

Valley Springs Bottled Water Recalled Due to Insanitary Conditions

Valley Springs recalled 379,868 units of bottled water on February 6, 2026. The recall affects multiple sizes and brands due to insanitary bottling conditions. Consumers should not consume the product and seek refunds or replacements.

Valley Springs Artesian Gold
Water was
Read more
Health & Personal Care
HIGH
FDA DEVICE

Hitachi Proton Beam Therapy Device Recalled for Software Issues

Hitachi Ltd. recalled one unit of its Proton Beam Therapy System on February 6, 2026 due to a software anomaly. The issue may result in positional discrepancies during patient treatment. The recall affects distribution in Texas and Washington D.C.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
Read more
Health & Personal Care
HIGH
FDA DEVICE

Hitachi Proton Beam Therapy System Recalled Due to Software Issue

Hitachi recalled its Proton Beam Therapy System on February 6, 2026, due to a software anomaly that may result in positional discrepancies. The recall affects one unit distributed in Texas and Washington D.C. Healthcare providers and patients must stop using the device immediately.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
Read more
Recalled Semfri Multi-Purpose Helmet - front view
HIGH
CPSC

Semfri Children's Helmets Recalled Over Serious Head Injury Risk

Semfri recalled children's helmets on February 5, 2026, due to safety violations. The helmets do not comply with mandatory safety standards, posing a serious risk of head injury. Consumers should stop using the helmets immediately and seek a refund.

Semfri Children's Helmets
The recalled
Read more
Previous
12345...86
Next

Tag Statistics

Total Recalls
1,716

Related Tags

immediate actionstop use immediatelyreturn for refundreplacement availablefda regulatedinfant productadult productelectronicbattery poweredlithium batteryvehiclenhtsa regulated