Health & Personal Care
HIGH
FDA DEVICE
Medline Recalled 7,913 Reprocessed ACUSON AcuNav Ultrasound Catheters for Intracardiac Imaging
Medline Industries, LP
Specific lots
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
Medline Reprocesses 7,913 Electrophysiology Catheters for Safety Risks
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls 7,913 Reprocessed ViewFlex Xtra ICE Catheters for Particulates (2025 Recall)
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Medline Livewire Steerable EP Catheters Recalled for Particulates in 2025 (7,913 Units)
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DEVICE
Fortress Introducer Sheath System 386594 Recall Expanded; 2,500 Units Worldwide Distribution (High-R
Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.
Fortress Introducer Sheath System
Units may
Health & Personal Care
HIGH
FDA DRUG
Exela Pharma Sciences 4.2% Sodium Bicarbonate Injection Recalled Over Arsenic Impurity Out-Of-Spec
Failed Impurities/Degradation Specifications: out of specification results for arsenic in the impurities tested.
SODIUM BICARBONATE
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DEVICE
Over 4,300 S.I.N. Implant EPIKUT Dental Implants Recalled Due to Quality Concerns
Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which could compromise product quality and performance.
S.I.N. Implant System Ltda
Dental implants
Health & Personal Care
HIGH
FDA DRUG
Pfizer Levoxyl Recall: Subpotent Levoxyl 50 mcg Tablets, 29,004 Bottles in U.S. Market (2025)
Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.
Levoxyl
Subpotent drug
Health & Personal Care
HIGH
FDA DEVICE
Ortho-Clinical Diagnostics Recalls 2,320 VITROS LAC Slides for Calibration Failures on XT Systems (W
Ortho-Clinical Diagnostics
VITROS Chemistry
Health & Personal Care
HIGH
FDA DRUG
Sucralfate Tablets Recall Expanded After CGMP Deviations; 26,992 Blister Packs Affected
SUCRALFATE
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems
Ortho-Clinical Diagnostics
VITROS Chemistry
Health & Personal Care
HIGH
FDA DEVICE
Ortoma AB Recalls 261 Inserter Adapters for Hip Cup Tools (2025)
Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.
Ortoma
Due to
Health & Personal Care
HIGH
FDA DEVICE
Merit Medical 10Fore Hemostasis Valve Recalled Due to Foreign Body Risk
Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.
Merit Medical Systems
Due to
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls 596 Flexicare BritePro Solo Fiber Optic Laryngoscope Handles in 2025
Medline Industries, LP recalled 596 Medline kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light may fail to illuminate as designed. Healthcare providers should stop using the devices immediately and follow recall instructions.
Medline Industries
Medline Industries,
Health & Personal Care
HIGH
FDA DRUG
Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.
DULOXETINE
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls 2,520 Kits With Flexicare Laryngoscope Handles Over Lighting Failure (2025)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.
Medline
Medline Industries,
Health & Personal Care
HIGH
FDA DEVICE
Zap Surgical Systems ZAP-X Radiosurgery System Recalled for 17 Units Worldwide in 2025
Zap Surgical Systems
If the
Health & Personal Care
HIGH
FDA DEVICE
Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)
Due to incorrect/lack of Unique Device Identifier (UDI) codes.
Home Health US
Due to
Health & Personal Care
HIGH
FDA DRUG
Cipla USA Albuterol Sulfate Inhalation Aerosol Recall Expanded for Stability Variance (2025)
Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point.
Cipla USA Inc.
Failed Stability
Health & Personal Care
HIGH
FDA DEVICE
Beckman Coulter MicroScan Neg MIC 56 Panels Recalled for Contamination Risk (2026)
Due to the likely presence of contamination in well(s).
Beckman Coulter
Due to
Health & Personal Care
HIGH
FDA DRUG
Taizhou Kangping Medical 3.85 Million Cartons of BZK Antiseptic Towelettes Recalled for Sterility LQ
Lack of Assurance of Sterility.
Taizhou Kangping Medical Science And Technology Co.
Lack of
Health & Personal Care
HIGH
FDA DRUG
Ascend Laboratories Amlodipine and Olmesartan Medoxomil Recall for Low Dissolution 8,568 Bottles in
Failed Dissolution Specifications: low dissolution results
Amlodipine and Olmesartan Medoxomil
Failed Dissolution
Health & Personal Care
HIGH
FDA DRUG
51,320 Belsomra Tablets Recalled for Delayed Dissolution Risk — Check Your Lot Numbers
Failed Dissolution Specifications: potential for delayed dissolution of the dose after administration which may result in delayed release of the drug, delaying onset of sleep.
Belsomra
Failed Dissolution
Health & Personal Care
HIGH
FDA DRUG
AUM Pharmaceuticals Isopropyl Alcohol Prep Pads Recall: 500 Cases Active, High Hazard
AUM Pharmaceuticals
cGMP Deviations
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