What’s the Problem?
According to the U.S. Food & Drug Administration (FDA), this recall affects the following products:
- 1000 Count Trazodone Tablets, USP — Lot# 36783 — Expiration Date 06/2022 — NDC# 42291-834
- 100 Count Sildenafil Tablets, USP — Lot# 36884 — Expiration Date 03/2022 — NDC# 42291-748
“Unintended intake of trazodone may result in adverse health consequences such as somnolence/sedation, dizziness, constipation, and blurred vision,” FDA said. “These adverse events may be more concerning in elderly patients due to a subsequent increased risk for falls and driving impairment.”
Trazodone hydrochloride is indicated for the treatment of major depressive disorder and sildenafil is the active ingredient in Viagra, which is a PDE-5 inhibitor used for the treatment of erectile dysfunction (ED).
If you were prescribed any drugs that are affected by this recall, you should discard them.
Any consumers who are concerned about a potential adverse reaction to Trazodone or Sildenafil should contact their healthcare provider immediately.
This recall began on December 9, 2020.
Do I Have a Trazodone Lawsuit?
The Pharmaceutical Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in Trazodone Lawsuits. We are handling individual litigation nationwide and currently accepting new injury and death cases in all 50 states.
If you or another loved one was injured by recalled Trazodone, you should contact our law firm immediately. You may be entitled to a settlement by filing a suit and we can help.