Recalls / 2023-03-16
Pfizer Recalls Nurtec ODT Prescription Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
23154 · Recalled 2023-03-16 · CPSC page

Description
This recall involves prescription drugs Nurtec ODT 75 mg orally disintegrating tablets sold in cartons containing one blister card of 8 tablets. The tablets are in a non-child resistant blister card packaged in a carton that includes the name of the product, dosage strength, expiration date. The dosage strength and expiration date are printed or stamped on the blister card. The recall includes the following: Product Description NDC Number Expiration Date Nurtec® ODT (rimegepant) 75mg 8-Unit Dose blister pack 72618-3000-2 All dates through 6/2026
Hazards
Reported injuries
Remedy
Products
| Name | Model | Units |
|---|---|---|
| Nurtec® ODT (rimegepant) orally disintegrating tablets, 75mg 8-Unit Dose blister pack | About 4.2 million |
Parties
- Manufacturers
- Biohaven Pharmaceuticals Inc., Pfizer Inc.
- Made in
- United States
- Sold at
- Pharmacies nationwide as a prescribed medicine, other factors.
Consumer contact
Pfizer at 800-879-3477 Monday through Friday 9 a.m. to 7 p.m. ET, online at www.pfizer.com/contact or online at www.Nurtec.com/PackagingUpdate or www.Nurtec.com and click "Recall to provide child resistant pouches to patients for storage of their medicine. Click for details" for more information.
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Source: CPSC recall 23154. Inclusion in this database is not legal or medical advice.