stop use immediately Recalls

2,228 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Recalled 15,438 Radiation Attenuation Vests Over Degradation Risk (2026)

Burlington Medical recalled 15,438 attenuation vests distributed worldwide after potential attenuation degradation over time. The vests use Xenolite 800 attenuation material and were produced between January 16, 2025 and January 21, 2026. Healthcare providers and patients should stop using the vest immediately and follow recall instructions.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

Waldemar Link GmbH & Co. KG recalls 74 Embrace Drill Tower devices distributed in 15 U.S. states. The recall notes mixed-up article numbers in the overview of the instruments. The surgical steps are correct. Stop using the device immediately and follow manufacturer instructions.

Waldemar Link GmbH & Co. KG
The surgical
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Embrace Shoulder Drill Tower Recalled After Mislabeling; 75 Units in 2026

Waldemar Link GmbH & Co. KG recalled 75 Embrace Shoulder Drill Tower devices distributed to U.S. hospitals after discovering mixed-up article numbers in the device overview. The surgical steps are correct, but the overview labeling is inaccurate. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions sent by email.

Waldemar Link GmbH & Co. KG
The surgical
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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
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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
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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
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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
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Food & Beverages
CRITICAL
FDA FOOD

Juniper Granola Junebar Peanut Chocolate Chip Snack Bar Recalled in 2026

Juniper Granola recalled 1,800 Junebar Peanut Chocolate Chip All Natural Snack Bars sold in New York after undeclared milk and soy were found. The product can cause severe allergic reactions in milk or soy allergic individuals. Stop using the bars and contact Juniper Granola for a refund or replacement.

Juniper Granola
Products contain
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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
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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
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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
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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
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific EndoVive PEG Kit Recalled for Sterility Risk in 806 Kits (2026)

Boston Scientific is recalling 806 EndoVive Safety PEG Kits sold nationwide. The recall concerns BD ChloraPrep Triple Swabsticks with open or compromised seals that could compromise sterility or dry the antiseptic solution. Hospitals and patients should stop using the kits immediately and follow the manufacturer's recall instructions.

Boston Scientific
Recall of
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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
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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
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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
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Food & Beverages
HIGH
FDA FOOD

Hortex Mieszanka 9 Recall for Glass Contamination in 2026

1,134 units of Hortex Mieszanka 9 Spring Vegetable Mix are recalled in Illinois due to potential glass contamination. The recall involves LOT SoC1070925 and UPC 5900477018735. Consumers should stop using the product and contact Polski Ogrod Sp. z o.o. for refunds or replacements.

Polski Ogrod
potential contamination
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Tag Statistics

Total Recalls
2,228

Related Tags

immediate actionreplacement availablereturn for refundfda regulatedcpsc regulatedmandatory standard violationsuffocation risklaceration riskelectrical hazardtip over riskpoisoning riskinfant product