Reported May 22, 2013 · Terminated
BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By
Performance Plus Marketing, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Performance Plus Marketing, Inc. · 5560 E 61st St · Commerce, CA · 90040-3406
Is this the product you have?
BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By
3 of 3 products
| Model / number | Barcodes | Product as published |
|---|---|---|
705105524764 | 5 count blister | |
736211124012 | 10 count blister | |
736211123916. | 736211123916 | — |
- Lot codes and dates
- 1
- count blisterLot# 01M0412
- Exp
04/15and Lot#91782
- Exp01/14. 5
- count blisterLot# 05M0412
- Exp
04/1510
- count blisterLot# 10M0412
- Exp04/15
- Amount recalled
- 213,000 capsules
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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