Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557
FDA Drug Recall #D-0452-2024 — Class I — March 19, 2024
Recall Summary
| Recall Number | D-0452-2024 |
| Classification | Class I — Serious risk |
| Date Initiated | March 19, 2024 |
| Status | Ongoing |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Pyramids Wholesale Inc. |
| Location | Los Angeles, CA |
| Product Type | Drugs |
| Quantity | 149 boxes |
Product Description
Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557
Reason for Recall
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Distribution Pattern
Nationwide in the USA
Lot / Code Information
All Lots
Other Recalls from Pyramids Wholesale Inc.
| Recall # | Classification | Product | Date |
|---|---|---|---|
| D-0449-2024 | Class I | Weiner Boner Honey, 12g packet, 100% Organic Fo... | Mar 19, 2024 |
| D-0450-2024 | Class I | Flower Power, CBD infused Female Enhancement, 5... | Mar 19, 2024 |
| D-0448-2024 | Class I | Spanish Fly 22K capsules, 2-count box, UPC 0 66... | Mar 19, 2024 |
| D-0451-2024 | Class I | Samurai-X Honey 6800, UPC 2 56891 27553 3. | Mar 19, 2024 |
| D-0457-2024 | Class I | ALPHASTRIP MALE PERFORMANCE ENHANCER, The faste... | Mar 19, 2024 |
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.