Health & Personal Care
HIGH
FDA DEVICE
Fisher & Paykel Recall 51,144 Airvo 2 and myAirvo 2 Humidifiers Over Power-Disconnect Audible Alert
Fisher & Paykel Healthcare
When unintentionally
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
B Braun Medical ESPOCAN Spinal/Epidural Tray Recalled Over Lid Position Risk
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL
Potential for
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Recall: 60-Unit Anesthesia Tray Recalled for Catheter Connector Lid Position Issue
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health 200 Salem Sump Gastroduodenal Tubes Recalled Worldwide for ARV Breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
Cardinal Health 200
Firm has
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid-Position Issue (21,270 Units)
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems LOGIQ P10 Ultrasound Systems Recalled for 65 Units in 2025 Over UGAP Data Errors
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.
GE Medical Systems
The Ultrasound-Guided
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Zenith Alpha 2 Thoracic Graft Recall Affects 695 Devices in 2025
Affected devices may contain PTFE coating scrapings. Scrapings could be released during device deployment, potentially causing intravascular embolization.
Cook Medical
Affected devices
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Recalls 2,840 Anesthesia Tray Kits Over Catheter Lid Defect (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Recall Expands for Perifix FX Epidural Tray and Catheter Over Lid Position Defect (Z
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Recall Expands for Epidural Tray and Catheter Over Lid Positioning Issue (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health 200 Salem Sump Stomach Tubes Recalled Worldwide in 2025 for ARV Breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
Cardinal Health 200
Firm has
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Recalls 0 CE17TKFSDT Epidural Tray Kit for Lid Position Hazard (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health 200 Recalls Salem Sump Dual-Lumen Stomach Tubes Over ARV Breakage (2025)
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
Cardinal Health 200
Firm has
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical PERIFIX FX Epidural Set Recalled for Lid-Position Defect in 2025
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health Salem Sump Stomach Tubes Recalled for ARV Breakage Risk (2025)
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
Cardinal Health
Firm has
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health Salem Sump PVC Tubes Recalled for ARV Breakage Risk (2025)
Cardinal Health 200, LLC recalled Salem Sump PVC Tubes worldwide after ARV breakage complaints. The anti-reflux valve can break under excessive force during use. Clinicians and patients should stop using the device and await recall instructions.
Cardinal Health 200
Firm has
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health 200 Salem Sump Anti-Reflux Valve Recalled for Breakage Risk (2025)
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
Cardinal Health
Firm has
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Perifix FX Epidural Tray Recall for Lid Misalignment in Catheter Connector
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL
Potential for
Health & Personal Care
HIGH
FDA DEVICE
HeartSine Pad-Pak Defibrillator Pads Recalled for 1,291,165 Units in 2025
Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.
HeartSine Technologies
Due to
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems LOGIQ P10 Ultrasound System Recalled for UGAP Data Inaccuracy (31 Units, 2025)
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.
GE Medical Systems
The Ultrasound-Guided
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems LOGIQ P9 R4.5 Ultrasound System Recalled for Inaccurate Liver Readings (37 Units)
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.
GE Medical Systems
The Ultrasound-Guided
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid Misalignment in 48,110 Units (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical PERIFIX FX Epidural Tray Recalled for 0 Units in 2025
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DRUG
Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025
CGMP Deviations: Market complaints received for gritty texture (grainy)
Glenmark Pharmaceuticals
CGMP Deviations:
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