All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical da Vinci S/Si EndoWrist Recall 6,152 Instruments for Pitch Cable Frays (2026)

Intuitive Surgical recalled 6,152 da Vinci S, Si Permanent Cautery Hook Instruments distributed to U.S. hospitals and clinics overseas. The defect involves frayed or broken pitch cables. Healthcare facilities should stop using the instruments immediately and follow manufacturer recall instructions. If you operate with these tools, consult your supplier or Intuitive Surgical for next steps.

Intuitive Surgical
Due to
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Vehicles & Parts
HIGH
NHTSA

Hyundai Palisade 2025 Seat Belt Buckle Recall Affects 2020-2025 Models

Hyundai Motor America recalls 2020-2025 Palisade SUVs sold through Hyundai dealers. The rear and other seat belt buckles may fail to latch. Owner notification letters are scheduled for November 10, 2025, and dealers will inspect and replace buckle assemblies at no cost.

Hyundai
Seat belt
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Vehicles & Parts
HIGH
NHTSA

Hyundai IONIQ 6 Recall Expands for Charging Port Door Detachment

Hyundai Motor America recalls 2023-2025 IONIQ 6 electric vehicles due to a charging port door panel that may detach. Dealers will apply adhesive as the remedy. Owner letters begin November 10, 2025. VINs searchable on NHTSA as of September 13, 2025.

Hyundai
A detached
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Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical da Vinci S, Si Grasping Retractor Instrument Recalled for 2,660 Units (2026)

Intuitive Surgical recalled 2,660 da Vinci S/Si Grasping Retractor Instruments worldwide after increased complaints of broken or frayed grip cables. The devices transmit motion from input disks to the distal tip and are used in robotic surgery. Hospitals and surgical centers should stop using the device immediately and follow recall instructions from the manufacturer.

Intuitive Surgical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard

Heraeus Medical GmbH recalled PALACOS R+G pro 40 and 80 bone cements on December 9, 2025. The recall follows multiple reports of ampoule breakage that prevent proper use of the product. Patients and healthcare providers must stop using the affected devices immediately.

Heraeus Medical GmbH
increase of
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Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical Recalls 2,095 da Vinci S, Si EndoWrist Tenaculum Forceps Instrument (2025)

Intuitive Surgical recalled 2,095 units of the da Vinci S, Si EndoWrist Tenaculum Forceps Instrument distributed nationwide in the United States and in multiple countries after reports of frayed or broken pitch cables. The defect can compromise instrument control during surgery. Hospitals and surgeons should stop using the device immediately and follow recall instructions from Intuitive Surgical.

Intuitive Surgical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical da Vinci S/Si Monopolar Curved Scissors Recall for 86,904 Units Worldwide (2025)

Intuitive Surgical recalled 86,904 da Vinci S and Si Monopolar Curved Scissors instruments sold worldwide to hospitals and surgical centers. The recall cites increased complaints of broken or frayed grip cables on reusable instruments. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.

Intuitive Surgical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical da Vinci S/Si Mega Needle Driver Instrument Recall 7,819 Units Worldwide (2026)

Intuitive Surgical recalled 7,819 units of the da Vinci S/Si Mega Needle Driver Instrument sold worldwide to hospitals and healthcare providers. The recall cites broken or frayed grip cables that can impair instrument control. Stop using the device and follow the manufacturer’s recall instructions for replacement or service.

Intuitive Surgical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Heraeus Medical Recalls PALACOS Bone Cement Due to Breakage Risk

Heraeus Medical GmbH recalled PALACOS MV+G pro 40 and MV+G pro 80 bone cement on December 9, 2025. The recall follows complaints about ampoule breakage, which can prevent proper cement formation. This issue could jeopardize patient safety during medical procedures.

Heraeus Medical GmbH
increase of
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Health & Personal Care
HIGH
FDA DEVICE

Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard

Heraeus Medical GmbH recalled PALACOS MV pro 40 and MV pro 80 bone cement on December 9, 2025. The recall follows numerous complaints about ampoule breakage. This defect can prevent proper cement dough formation, rendering the product unusable for patients.

Heraeus Medical GmbH
increase of
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Health & Personal Care
HIGH
FDA DEVICE

Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage

Heraeus Medical GmbH recalled PALACOS R pro 40 and R pro 80 bone cement on December 9, 2025. The recall follows multiple complaints of ampoule breakage affecting product usability. Healthcare providers must stop using the product immediately.

Heraeus Medical GmbH
increase of
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Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion Systems Recalled Due to Software Issues

Philips recalled 990 Azurion Systems on December 8, 2025, after nine software issues were identified. The defects may cause loss of X-ray functionality, system restarts, and other operational failures. Healthcare providers must stop using the devices immediately.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Nine (9)
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Food & Beverages
HIGH
FDA FOOD

Sam Dry Fruits Pistachio Meats Recalled Due to Salmonella Risk

Sam Dry Fruits & Nuts Enterprises recalled 32,610 pounds of pistachio meats on December 8, 2025. The recall stems from potential Salmonella contamination. Consumers should not consume the product and seek a refund.

Sam Dry Fruits and Nuts Enterprises
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Goldenroot Ginger Beer Recalled Over Pasteurization Issue

Goldenroot recalled 421 cases of Lemon Ginger Jalapeno Ginger Beer on December 8, 2025. The recall stems from potential unpasteurized ginger juice, posing a health risk. Consumers should not consume the product and seek refunds immediately.

Weaver's Brew
Ginger Beer
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Health & Personal Care
HIGH
FDA DRUG

ORL Labs Recalls Kids Mouthwash Over cGMP Deviations

ORL Labs, LLC recalled 570 bottles of ORL Kids Mouthwash, Bubblegum Flavor on December 8, 2025. The recall stems from violations of current Good Manufacturing Practices (cGMP). The product was distributed only in Arizona and poses potential safety risks for children.

ORL Labs
cGMP Deviations
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Food & Beverages
HIGH
FDA FOOD

Goldenroot Ginger Beer Recalled Over Pasteurization Issues

Goldenroot recalled 649 cases of Yuzu Ginger Lemongrass Ginger Beer on December 8, 2025. The product may contain ginger juice that did not undergo required pasteurization. Consumers should not consume it and seek refunds from Weaver's Brew LLC.

Weaver's Brew
Ginger Beer
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls LDL Cholesterol Assay Due to Performance Issues

Beckman Coulter recalled 34,451 units of its LDL Cholesterol OSR6x96 assay on December 8, 2025, due to significant performance interference. The recall affects multiple states in the U.S. and several countries internationally. Affected products may provide inaccurate LDL cholesterol readings, posing health risks to patients.

Beckman Coulter Ireland
Beckman Coulter
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Food & Beverages
HIGH
FDA FOOD

Weaver's Brew Ginger Beer Recalled Over Pasteurization Issues

Weaver's Brew recalled 1,014 cases of Lemon Ginger Hibiscus Ginger Beer on December 8, 2025. The product might contain unpasteurized ginger juice, posing a high health risk. Consumers should not consume the product and should seek refunds.

Weaver's Brew
Ginger Beer
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Food & Beverages
HIGH
FDA FOOD

Goldenroot Ginger Beer Recalled for Pasteurization Failure

Goldenroot recalled 1,070 cases of Lemon Double Ginger Beer on December 8, 2025. The ginger beer may contain unpasteurized ginger juice, posing a health risk. Consumers should not consume the product and seek refunds immediately.

Weaver's Brew
Ginger Beer
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