1,734 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
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Medline Industries recalled 7,913 reprocessed ViewFlex Xtra ICE catheters on July 31, 2025. The recall affects specific lots due to potential residual particulates that may cause serious health risks. Patients and healthcare providers must stop using the devices immediately.
Medline Industries recalled 7,913 reprocessed AcuNav Ultrasound Catheters on July 31, 2025. The devices may contain harmful residual particulates that pose an infection risk. Patients and healthcare providers should stop using these devices immediately and follow recall instructions.
Medline Industries recalled 7,913 electrophysiology catheters on July 31, 2025, due to contamination concerns. Specific lots may contain small residual particulates, posing risks of systemic infection and thrombus formation. Patients and healthcare providers should stop using these devices immediately.
Medline Industries recalled 7,913 reprocessed electrophysiology catheters on July 31, 2025. The recall affects specific lots that may contain harmful particulates. Using these catheters could lead to serious health risks including embolism or deep vein thrombosis.
Medline Industries recalled 7,913 reprocessed electrophysiology catheters on July 31, 2025. Residual particulates on patient-contacting surfaces pose a risk of serious infection and thrombus formation. Patients and healthcare providers must stop using these devices immediately.
Exela Pharma Sciences recalled 4.2% Sodium Bicarbonate Injection on July 30, 2025, due to arsenic contamination. The recall affects single-dose vials distributed nationwide. Consumers and healthcare providers must stop using the product immediately.
Contract Medical International GmbH recalled 2,500 Fortress Introducer Sheath Systems on July 30, 2025. Units may have incorrect pouch labeling, leading to potential use of the wrong device version. Patients and healthcare providers should stop using the product immediately.
S.I.N. Implant System Ltda recalled 4,367 dental implants on July 30, 2025, due to improper storage conditions. The recalled products may have compromised packaging, affecting their quality and performance. Patients and healthcare providers should stop using these devices immediately.
American Health Packaging recalled 26,992 blister packs of Sucralfate Tablets on July 29, 2025. The recall follows CGMP deviations that affect product quality. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Ortho-Clinical Diagnostics recalled 2,320 units of VITROS Chemistry Products LAC Slides on July 29, 2025. Calibration failures in lots from coating 0130 and above delay test results and may impact patient management. Healthcare providers and patients must stop using these slides immediately.
Pfizer Inc. recalled 29,004 bottles of Levoxyl on July 29, 2025, due to subpotency. The recall affects levothyroxine sodium tablets, 50 mcg, Rx only, distributed in the U.S. Consumers should stop using the product immediately.
Ortho-Clinical Diagnostics recalled 2,908 units of VITROS Chemistry Products LAC Slides on July 29, 2025. The recall affects lots from coating 0130 and above due to increased calibration failures that delay test results. The issue may impact patient management and was identified through an uptick in customer complaints.
ORTOMA AB recalled 261 Inserter Adapters on July 28, 2025, due to a potential weld failure. The defect poses a risk of improper positioning during hip implant procedures. The recall affects devices distributed worldwide, including the U.S. and countries like Japan and Sweden.
Medline Industries, LP recalled 596 medical convenience kits on July 25, 2025. The recall affects kits with Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to light failure. Patients and healthcare providers must stop using these devices immediately.
Medline Industries, LP recalled 2,520 medical convenience kits on July 25, 2025. The recall affects multiple intubation trays containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light in these devices fails to illuminate, posing a serious risk in emergency situations.
Merit Medical Systems recalled 447 units of the 10Fore Hemostasis Valve on July 25, 2025. A manufacturing issue may cause a deformed silicone quad ring, posing a risk of foreign body in the fluid pathway. This recall affects the U.S. and Canada.
Towa Pharmaceutical Europe recalled 1,856 bottles of Duloxetine delayed-release capsules on July 25, 2025. The recall follows the discovery of N-nitroso-duloxetine impurity exceeding FDA limits. Consumers should stop using the product immediately and seek guidance.
Zap Surgical Systems recalled 17 ZAP-X Radiosurgery Systems on July 25, 2025. A software defect may cause the collimator to collide with patients during operation. Healthcare providers should stop using the device immediately.
Home Health US recalled 4,661 sterile lancets on July 25, 2025. The recall stems from incorrect or missing Unique Device Identifier (UDI) codes. Affected products were distributed nationwide through Amazon.
Diamond G Forest Products recalled turpentine bottles on July 24, 2025, due to a risk of child poisoning. The 4-ounce glass bottles lack child-resistant packaging, violating safety standards. The recall affects an unspecified number of bottles sold nationwide.
Creekwood Naturals recalled Gum Spirits of Turpentine bottles due to non-compliance with child-resistant packaging standards. The recall affects bottles sold since July 2025. Consumers should secure this product away from children immediately.
Cipla USA, Inc. recalled 20,352 packs of Albuterol Sulfate inhalation aerosol on July 24, 2025. The recall follows out-of-specification results in particle size distribution during stability testing. Consumers must stop using the product immediately.
Beckman Coulter recalled 685 boxes of MicroScan Neg MIC 56 panels distributed nationwide to U.S. healthcare facilities after contamination was reported in wells. Contamination could lead to unreliable antimicrobial susceptibility and organism-identification results. Health care providers should stop using the panels and follow Beckman Coulter recall instructions immediately.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes on July 22, 2025. The recall stems from a lack of assurance of sterility, posing a high risk to users. Consumers and healthcare providers must stop using these towelettes immediately.
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