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“Today The World” is voluntarily recalling two lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules to the consumer level. FDA analysis has found the products to contain undeclared Tadalafil and Nortadalafil (structurally similar to Tadalafil). Tadalafil and Nortadala
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FDA Roundup: February 2, 2024
FDA Roundup: February 2, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-february-2-2024
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Do Not Use Cardinal Health Monoject Syringes with Syringe Pumps and PCA Pumps – Letter to Health Care Providers
Cardinal Health Monoject syringes have demonstrated recognition and compatibility issues with certain infusion pumps.
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Insight Pharmaceuticals Issues Voluntary Nationwide Recall of TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid Due to the Presence of Benzene
Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company (“Insight”), is voluntarily recalling two lots of TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid to the consumer level. A recent review by our manufacturer and their third-party lab found that samples from two lot
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Cardinal Health Recalls Monoject Disposable Syringes for Incompatibilities with Syringe Pumps
Some Cardinal Health Monoject Luer-lock tip syringes have demonstrated recognition and compatibility issues with certain syringe infusion pumps.
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Maquet Cardiovascular, LLC Recalls Atrium Express Dry Suction Dry Seal Chest Drain Containing Sterile Water Based Products Under Recall by Nurse Assist
Maquet Express Chest Drain recalled over sterility concerns. When used without the provided syringe, the Express chest drains are safe to use.
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UPDATE: Certain Philips Respironics Ventilators, BiPAP Machines, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication
This update provides additional information on the recall and recommendations for people who use repaired and replaced devices.
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FAQs on Philips Respironics Ventilator, BiPAP Machine, and CPAP Machine Recalls
Find answers to frequently asked questions on Philips Respironics ventilators, BiPAP, and CPAP machines recall
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FDA Roundup: January 30, 2024
FDA Roundup: January 30, 2024
http://www.fda.gov/news-events/press-announcements/fda-roundup-january-30-2024
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Globus Medical, Inc. Recalls ExcelsiusGPS Flat Panel Fluoroscopy Registration Fixture Due to a Calibration Error
Globus Medical, Inc. is recalling the ExcelsiusGPS, an imaging device, due to a calibration algorithm error that may affect the accuracy of implant placement.