Nystatin Topical Powder, USP, 100,000 USP units per gram, 15 grams per bottle, Rx only, Vensun, N...
FDA Drug Recall #D-1059-2017 — Class II — May 17, 2017
Recall Summary
| Recall Number | D-1059-2017 |
| Classification | Class II — Moderate risk |
| Date Initiated | May 17, 2017 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | X-Gen Pharmaceuticals Inc. |
| Location | Horseheads, NY |
| Product Type | Drugs |
| Quantity | 9,816 bottles |
Product Description
Nystatin Topical Powder, USP, 100,000 USP units per gram, 15 grams per bottle, Rx only, Vensun, NDC 42543-052-61
Reason for Recall
Presence of Foreign Substance: potential presence of plastic particles.
Distribution Pattern
Nationwide in the US
Lot / Code Information
Lot #: 23701.158A, EXP 10/31/18
Other Recalls from X-Gen Pharmaceuticals Inc.
| Recall # | Classification | Product | Date |
|---|---|---|---|
| D-0434-2024 | Class III | Cyclophosphamide for Injection, USP, 1g/vial, L... | Apr 2, 2024 |
| D-0433-2024 | Class III | Cyclophosphamide for Injection, USP, 500mg/vial... | Apr 2, 2024 |
| D-0328-2021 | Class II | Neomycin Sulfate Tablets, USP 500mg, Rx Only, 1... | Mar 19, 2021 |
| D-0519-2020 | Class III | Levetiracetam Injection, 500 mg/5mL, 10 single-... | Oct 11, 2019 |
| D-1084-2019 | Class III | Clonidine HCL Injection, 1000 mcg/10mL (100 mcg... | Mar 29, 2019 |
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.