Pfizer Nurtec ODT Prescription Drugs Recall
Failure to Meet Child Resistant Packaging Requirement.
CPSC recall #23154 · announced Mar 16, 2023 · verified Jul 30, 2026


How to identify the recalled product
| Product | Nurtec® ODT (rimegepant) orally disintegrating tablets, 75mg 8-Unit Dose blister pack |
| Manufacturer / importer | Biohaven Pharmaceuticals Inc., of New Haven, Conn.; Pfizer Inc., of New York |
| Units recalled | About 4.2 million |
The recall
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
Reported incidents
None reported
What consumers should do now
Stop using the recalled product immediately. Contact the company for the announced remedy. Do not resell or donate recalled products — it is illegal under federal law.
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.
Source: U.S. Consumer Product Safety Commission. Official notice title: “Pfizer Recalls Nurtec ODT Prescription Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning”. Read the official CPSC notice