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FDA / Product Alerts
- Baxter Home Choice Class I Recall New!
- Recall-One Touch SureStep Test Strips New!
- Dexferrum (iron dextran injection) Labeling Change New!
- Philips AED Recall
- New USP Heparin Standards
- Digoxin Voluntary Recall Notification
- Hach SteriChek Recall Notification
- Heparin Recall Alert
- Heparin Recall Alert Follow-Up
- Heparin Recall Alert Update 1
- Heparin Recall Alert Update 2
- NxStage Product Recall Letter to State Surveryors
- NxStage Product Recall Product List
- USFDA Information on ESAs
- USFDA Update on MRI Contrast Agents Containing Gadolinium and Nephrogenic Fibrosing Dermopathy
- Voluntary Recall of Epoetin Alfa (PROCRIT)
- Class 1 Recall: Physio Control, Inc. LifePak CR Plus Automated External Defibrillators (AEDs)
- FDA warning regarding glucose testing for PD Patients
- FDA Public Health Notification: Potentially Fatal Errors with GDH-PQQ* Glucose Monitoring Technology (glucose dehydrogenase pyrroloquinoline quinine)
- Voluntary Nationwide Recall of Accusure Insulin Syringes
- Class I Recall: Physio-Control Inc., LIFEPAK CR Plus Automated External Defibrillators (AEDs)
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Last Updated: 08/27/2010
