Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020
Reported: May 22, 2019 Initiated: April 23, 2019 #D-1292-2019
Product Description
Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020
Reason for Recall
Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Details
- Recalling Firm
- D.B.P. Distribution
- Units Affected
- unknown
- Distribution
- Nationwide.
- Location
- Chatsworth, CA
Frequently Asked Questions
What product was recalled? ▼
Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020. Recalled by D.B.P. Distribution. Units affected: unknown.
Why was this product recalled? ▼
Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 22, 2019. Severity: Critical. Recall number: D-1292-2019.
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