Health & Personal Care
HIGH
FDA DEVICE
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
Due to
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
HIGH
FDA DEVICE
Intuitive Surgical da Vinci S/Si Mega Needle Driver Instrument Recall 7,819 Units Worldwide (2026)
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Intuitive Surgical
Due to
Health & Personal Care
HIGH
FDA DEVICE
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
Due to
Health & Personal Care
HIGH
FDA DEVICE
Intuitive Surgical da Vinci S/Si Monopolar Curved Scissors Recall for 86,904 Units Worldwide (2025)
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Intuitive Surgical
Due to
Health & Personal Care
HIGH
FDA DEVICE
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
Intuitive Surgical
Due to
Health & Personal Care
HIGH
FDA DEVICE
Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard
Heraeus Medical GmbH
increase of
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
Health & Personal Care
HIGH
FDA DEVICE
Heraeus Medical Recalls PALACOS Bone Cement Due to Breakage Risk
Heraeus Medical GmbH
increase of
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
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion Systems Recalled Due to Software Issues
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Nine (9)
Health & Personal Care
HIGH
FDA DRUG
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.
ORL Labs
cGMP Deviations
Health & Personal Care
HIGH
FDA DEVICE
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
Securitas Healthcare
Health & Personal Care
HIGH
FDA DEVICE
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.
Securitas Healthcare
Securitas Healthcare
Health & Personal Care
HIGH
FDA DEVICE
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.
IMRIS Imaging
Torque screw
Health & Personal Care
HIGH
FDA DEVICE
Beckman Coulter Recalls LDL Cholesterol Assay Due to Performance Issues
Beckman Coulter Ireland
Beckman Coulter
Health & Personal Care
HIGH
FDA DEVICE
Siemens Recalls LUMINOS Medical Imaging Systems Over Collimation Risk
Siemens Medical Solutions USA
A potential
Health & Personal Care
HIGH
FDA DEVICE
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.
Meridian Bioscience
The affected
Health & Personal Care
HIGH
FDA DEVICE
LimFlow Vector Medical Device Recalled Due to Expiration Date Error
LimFlow
Incorrect expiration
Health & Personal Care
HIGH
FDA DEVICE
Beaver-Visitec Recalls Laser and Endoscopy System Over Safety Hazard
Beaver-Visitec International
Manufacturing deviation
Health & Personal Care
HIGH
FDA DEVICE
Intuitive Surgical Recalls Ion Vision Probe Bag Over Sterility Risk
Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Intuitive Surgical
Due to
Health & Personal Care
HIGH
FDA DEVICE
Mobius Imaging Recalls AIRO CT X-ray Pendant Due to Safety Risk
AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.
Mobius Imaging
AIRO pendant
Health & Personal Care
HIGH
FDA DEVICE
Merit Medical Recalls Custom Procedure Kits Due to Detachment Hazard
Inflation device handle may detach from the syringe during procedure.
Merit Medical Systems
Inflation device
Health & Personal Care
HIGH
FDA DEVICE
Merit Medical Systems Recalls Angioplasty Packs Over Detachment Hazard
Inflation device handle may detach from the syringe during procedure.
Merit Medical Systems
Inflation device
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