Triamcinolone Acetonide (pf recalls
The FDA has published 3 recalls involving Triamcinolone Acetonide (pf since 2014. The latest was reported on 11 Mar 2020. Most were for sterility. Fusion IV Pharmaceuticals has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls3since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 11 Mar 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why triamcinolone acetonide (pf is recalled
Companies
By year
All triamcinolone acetonide (pf recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Triamcinolone Acetonide (PF) Injectable Suspension recalled | Fusion IV Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Triamcinolone Acetonide (PF) Injectable Suspension recalled | Fusion IV Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Triamcinolone acetonide (PF) 40 mg/mL injection suspension recalled | Martin Avenue Pharmacy | Sterility | Nationwide |
Should you stop taking Triamcinolone Acetonide (pf?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.