cpsc regulated Recalls

Intuitive Surgical recalls 2,370 da Vinci S/Si Double Fenestrated Grasper Instruments (2026)

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

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

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

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.

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.

Heraeus Medical Recalls PALACOS Bone Cement Due to Breakage Risk

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.

ORL Labs Recalls Kids Mouthwash Over cGMP Deviations

Beckman Coulter Recalls LDL Cholesterol Assay Due to Performance Issues

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.

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.

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

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.

Honda Pilot, Acura TLX and MDX Recalled for Faulty Brake Pedal Pivot Pin (2025)

Keurig Recalls McCafe Decaf Coffee Pods Due to Caffeine Risk

Keurig Green Mountain recalled 960 cartons of McCafe Premium Roast Decaf Coffee K-Cup Pods on December 6, 2025. The product is inaccurately labeled as decaf but may contain caffeine. Consumers in CA, IN, and NV should not consume the pods and seek refunds.

Siemens Recalls LUMINOS Medical Imaging Systems Over Collimation Risk

Meridian Bioscience Recalls Revogene C. difficile Assay Over False-Negative Risk

The affected lots show a decline in performance over time, which may lead to false-negative results.

LimFlow Vector Medical Device Recalled Due to Expiration Date Error

Bharat Bazar Recalls Asafoetida Due to Undeclared Wheat