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1 Οκτ 2024 · Recalls, Market Withdrawals, & Safety Alerts. The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Not all...
- Enforcement Reports
Separate from determining whether a firm’s action meets the...
- Industry Guidance For Recalls
The .gov means it’s official. Federal government websites...
- Major Product Recalls
Recalls associated with Almark’s recall of hard-boiled egg...
- Archive for Recalls, Market Withdrawals & Safety Alerts
The Recalls, Market Withdrawals & Safety Alerts are...
- Enforcement Reports
ABC News’ Dr. Darien Sutton tells us what to know about the recall due to the inclusion of a chemical that is not FDA approved, and sent nearly 50 people to the hospital. 4 months ago.
16 Απρ 2024 · The U.S. Food and Drug Administration has announced a recall for a pair of heart devices that have been linked to hundreds of injuries and at least 14 deaths. ABC News Video
13 Ιουν 2024 · The Food and Drug Administration failed to heed warning signs that there were mounting concerns with one of the nation's largest infant formula makers, as a series of babies' severe illnesses and ...
FDA Approved: No. Brand name: Exanta. Generic name: ximelagatran. Company: AstraZeneca. Treatment for: Prevention of Thromboembolism in Atrial Fibrillation. Exanta (ximelagatran) is an investigational oral direct thrombin inhibitor (oral DTI) intended for use in the prevention of strokes in patients with atrial fibrillation, for the prevention ...
29 Οκτ 2024 · Dr. Elder: Yes. A class I recall is the most serious, where there is a reasonable probability that using or being exposed to the recalled drug will cause serious adverse health consequences for a ...
FDA news releases, media contacts, speeches, meetings and workshops, and other ways that FDA engages with the public.