All Product Recalls

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

Due to increased complaints for broken/frayed grip cables for reusable instruments.

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

Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

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

Hyundai Motor America (Hyundai) is recalling certain 2020-2025 Palisade vehicles. The seat belt buckles in the driver, passenger, and second-row window seats may fail to latch.

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 IONIQ 5 2025 Recall for Rear Suspension Bolts Affects Stability Control

Hyundai Motor America (Hyundai) is recalling certain 2025 IONIQ 5 electric vehicles. Certain rear suspension alignment adjustment bolts may have been improperly tightened, which can cause a loss of vehicle stability control.

Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard

Heraeus Medical Recalls PALACOS Bone Cement Due to Breakage Risk

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 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.

IMRIS Imaging Recalls Head Fixation Device Over Safety Concerns

IMRIS Imaging recalled 122 Head Fixation Devices on December 8, 2025. A torque screw may crack or separate, posing serious risks during surgical procedures. Healthcare providers must stop using the device and follow recall instructions immediately.

Goldenroot Ginger Beer Recalled Over Pasteurization Issues

Goldenroot recalled 1,066 cases of Lemon Ginger Elderberry Ginger Beer on December 8, 2025. The product may contain unpasteurized ginger juice, posing a health risk. Consumers should stop using the product immediately and seek a refund or replacement.

Securitas Healthcare Recalls 900 MHz Call Stations Over Firmware Issue

Securitas Healthcare recalled 5,627 Arial 900 MHz Call Stations on December 8, 2025. A firmware issue may prevent low battery alerts from being transmitted, posing a risk. Affected devices were sold worldwide, including the US and Canada.

Securitas Healthcare Recalls 900 MHz Call Station Over Battery Alert Failure

Securitas Healthcare recalled 1,898 units of the Arial 900 MHz Call Station on December 8, 2025. A firmware issue may prevent low battery alerts, posing a risk of battery failure. Users should stop using the device immediately and follow recall instructions.

ORL Kids Toothpaste Recalled Due to cGMP Deviations

ORL Labs recalled 1,458 containers of ORL Kids Natural Toothpaste, Bubblegum Flavor, on December 8, 2025. The recall follows cGMP deviations that could pose health risks. Consumers should stop using the product immediately.

Beckman Coulter Recalls LDL Cholesterol Assay Due to Performance Issues

ORL Labs Recalls Kids Mouthwash Over cGMP Deviations

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.

Philips Azurion Systems Recalled Due to Software Issues

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 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.