Triamcinolone Diacetate Injectable Suspension recalled over labeling errors
- Recall date
- February 2, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Isomeric Pharmacy Solution, LLC recalls Triamcinolone Diacetate Injectable Suspension, 40 mg/mL, 10mL Multi-Dose Vial for Injection, Rx only, Isomeric Pharmacy…
- Recall number
- D-0728-2016
- FDA classification
- Class III
- Brand / firm
- Isomeric Pharmacy Solution, LLC
- Sold / distributed
- Nationwide
Why it was recalled
Labeling: Incorrect or Missing Lot and/or Exp Date: some vials may be mislabeled with an incorrect "Compounded" date, lot number, and "Do Not Use Beyond" date or BUD (Before Use Date) that may be longer than intended.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Triamcinolone Diacetate Injectable Suspension, 40 mg/mL, 10mL Multi-Dose Vial for Injection, Rx only, Isomeric Pharmacy Solutions, 2401 Foothill Dr., Salt Lake City, UT 84109
Get recall alerts
Free email alert whenever Isomeric Pharmacy Solution, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Isomeric Pharmacy Solution, LLC