VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com
Reported: December 11, 2024 Initiated: November 4, 2024 #D-0083-2025
Product Description
VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com
Reason for Recall
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
Details
- Recalling Firm
- Boulla LLC
- Units Affected
- Unknown
- Distribution
- Nationwide within the United States
- Location
- Sacramento, CA
Frequently Asked Questions
What product was recalled? ▼
VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com. Recalled by Boulla LLC. Units affected: Unknown.
Why was this product recalled? ▼
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 11, 2024. Severity: Critical. Recall number: D-0083-2025.
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