iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, S...

FDA Drug Recall #D-0981-2015 — Class I — January 25, 2015

Recall Summary

Recall Number D-0981-2015
Classification Class I — Serious risk
Date Initiated January 25, 2015
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Detox Transforms
Location Garner, NC
Product Type Drugs
Quantity 200 bottles

Product Description

iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00408 2.

Reason for Recall

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making iNSANE an unapproved drug.

Distribution Pattern

WV who distributed Nationwide.

Lot / Code Information

Lot: 0000:02, Exp 06/20/17

Other Recalls from Detox Transforms

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D-0979-2015 Class I AMPD GOLD Bee Pollen capsules, 350 mg, 60-count... Jan 25, 2015
D-0977-2015 Class I EDGE Amplified Weight Release capsules, 400 mg,... Jan 25, 2015
D-0980-2015 Class I BtRiM Max capsules, 60-count bottle, Developed ... Jan 25, 2015
D-0978-2015 Class I iNDiGO capsules, 220 mg, 60-count bottle, Deve... Jan 25, 2015

Frequently Asked Questions

Stop taking the medication and contact your pharmacist or doctor immediately. For Class I recalls, this is urgent. For Class II or III recalls, consult your doctor before stopping — abruptly discontinuing certain medications (blood pressure drugs, antidepressants, diabetes medications) can be more harmful than continuing while arranging a replacement. Check whether the recall applies to your specific lot number and expiration date. Return the product to your pharmacy and report any adverse effects to FDA MedWatch at 1-800-FDA-1088.

Not necessarily. Many drug recalls are initiated because of quality system failures or test results that suggest a product might not meet specifications — even if no patients have reported harm. The FDA uses a precautionary approach: if there is reason to believe quality standards were not met, a recall is required regardless of whether adverse effects have been reported. Class I recalls typically involve a reasonable probability of harm; Class II recalls may cause temporary health issues; Class III recalls are for products unlikely to cause adverse health consequences but that still violate regulations.

Pharmacies typically receive recall notices directly from drug wholesalers and manufacturers within days of the recall being announced. Your pharmacist can look up whether any product in your prescription history matches a recalled lot number. For current recalls, the FDA publishes updates at FDA.gov/safety/recalls-market-withdrawals-safety-alerts and sends MedWatch email alerts for significant drug safety issues. You can sign up for MedWatch alerts at FDA.gov. Most major pharmacy chains also have their own recall notification systems that automatically alert pharmacists when a recalled product is in their inventory.

What Should You Do?

Stop using this medication if affected by this recall. Contact your pharmacist or prescribing doctor immediately for guidance. Do not flush medications — use a drug take-back program.