Asenapine Sublingual Tablets, 5 mg, Rx Only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, ...
FDA Drug Recall #D-0379-2021 — Class III — April 19, 2021
Recall Summary
| Recall Number | D-0379-2021 |
| Classification | Class III — Low risk |
| Date Initiated | April 19, 2021 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | SigmaPharm Laboratories LLC |
| Location | Bensalem, PA |
| Product Type | Drugs |
| Quantity | 6266 bottles |
Product Description
Asenapine Sublingual Tablets, 5 mg, Rx Only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020 NDC 42794-016-10.
Reason for Recall
Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent
Distribution Pattern
Nationwide in the US
Lot / Code Information
Lots # 2012501, 2012601 , 2012701, & 2100701, Exp. AUG 2022
Other Recalls from SigmaPharm Laboratories LLC
| Recall # | Classification | Product | Date |
|---|---|---|---|
| D-0898-2021 | Class II | Sodium Phenylbutyrate Powder, 250 Grams, Rx Onl... | Sep 21, 2021 |
| D-0766-2021 | Class II | Sodium Phenylbutyrate POWDER, 250 grams bottle,... | Aug 13, 2021 |
| D-0380-2021 | Class III | Asenapine Sublingual Tablets, 10 mg, Rx only, 6... | Apr 19, 2021 |
| D-1344-2014 | Class II | Liothyronine Sodium Tablets, USP 5 mcg, Rx Only... | Apr 22, 2014 |
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.