Reported May 28, 2014 · Terminated
NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles,…
Tendex
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: Tendex · 311 Robertson Blvd · Beverly Hills, CA · 90211
Is this the product you have?
NATURECT Capsules Dietary Supplement 500 mgsupplied in 1 count blister pack and 51020and 40- count bottlesDistributed by P-BoostLos AngelesCA 900466
- Lot codes and dates
- Lot # F51Q
- EXP07/16
- The UPC Codes for Naturect are1ct- 893020242013 5ct - 893020242051 10ct - 893020242105 20ct - 893020242204 40ct - 893020242402
- Amount recalled
- unknown
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient, tadalafil, thus making these products unapproved drugs.
Using this product could cause serious injury, illness or death — stop using it now.
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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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