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FDA Safety Information on Drugs & Medical Devices

May 8, 2017Newsgaladmin

Early Alert: Endoscope Accessories Forceps/Irrigation Plug Issue from Olympus
Source: FDA MedWatch Safety Alert Published on 2024-12-23 By FDA
Alcon Laboratories Issues Voluntary Nationwide Recall of One (1) Lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101), Due to Fungal Contamination
Source: FDA MedWatch Safety Alert Published on 2024-12-23 By FDA
Early Alert: Nephroscope Sheath Issue from Trokamed GmbH
Source: FDA MedWatch Safety Alert Published on 2024-12-20 By FDA
Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution (EPINEPHrine Nasal Solution, USP) Due to the Potential for Administration Errors
Source: FDA MedWatch Safety Alert Published on 2024-12-20 By FDA
Implantable Marker Recall: Hologic Removes BioZorb 3D Bioabsorbable Markers due to Risk for Patient Complications
Source: FDA MedWatch Safety Alert Published on 2024-12-18 By FDA
Catheter Correction: Boston Scientific Updates Use Instructions for POLARx and POLARx FIT Cryoablation Balloon Catheters due to Higher than Anticipated Number of Reports of Atrio-Esophageal Fistula
Source: FDA MedWatch Safety Alert Published on 2024-12-18 By FDA
Shoppers-Plaza Issues Voluntary Nationwide Recall of Fouzee Sugarlin Herbal Formula Due To Presence Of Undeclared Metformin And Glyburide
Source: FDA MedWatch Safety Alert Published on 2024-12-18 By FDA
Accolade Pacemaker Devices by Boston Scientific and Potential Need for Early Device Replacement - FDA Safety Communication
Source: FDA MedWatch Safety Alert Published on 2024-12-16 By FDA
Buy-herbal.com Issues Voluntary Nationwide Recall of Nhan Sam Tuyet Lien Truy Phong Hoan Capsules Due to Undeclared Furosemide, Dexamethasone and Chlorpheniramine
Source: FDA MedWatch Safety Alert Published on 2024-12-13 By FDA
Ocaliva (obeticholic acid) by Intercept Pharmaceuticals: Drug Safety Communication - Serious Liver Injury Being Observed in Patients without Cirrhosis
Source: FDA MedWatch Safety Alert Published on 2024-12-12 By FDA
Early Alert: Infusion Pump Issue from Fresenius Kabi USA
Source: FDA MedWatch Safety Alert Published on 2024-12-11 By FDA
Neonatal Incubator Correction: GE HealthCare Updates Use Instructions for GE HealthCare Giraffe OmniBed Carestation and Incubator Carestation due to Risk of Patient Formaldehyde Exposure
Source: FDA MedWatch Safety Alert Published on 2024-12-06 By FDA
Syringe Recall: Cardinal Health Removes Certain Monoject U-100 mL Insulin Syringe Luer Lock with Tip Cap Soft Packs due to Incompatibility with Needleless Connectors
Source: FDA MedWatch Safety Alert Published on 2024-12-04 By FDA
Biopsy Needle Recall: Elekta Removes Disposable Biopsy Needle Kits due to Risk of Microscopic Stainless Steel Debris Inside Needle
Source: FDA MedWatch Safety Alert Published on 2024-11-29 By FDA
Peritoneal Dialysis Set Correction: Baxter Issues Correction for MiniCap Extended Life Peritoneal Dialysis Transfer Sets Due to Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA and/or NDL-PCBs
Source: FDA MedWatch Safety Alert Published on 2024-11-29 By FDA

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