Nurtec® ODT (rimegepant) orally disintegrating tablets, 75mg 8-Unit Dose blister pack
Summary
CPSC recall: Nurtec® ODT (rimegepant) orally disintegrating tablets, 75mg 8-Unit Dose blister pack. By Biohaven Pharmaceuticals Inc., of New Haven, Conn.. Hazard: The recalled prescription drugs must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.. Remedy: Consumers should immediately secure the recalled product out of the si
Details
Source
CPSC Consumer Product Recall
External ID
9565
Action Date
2023-03-16
Status
Recalled
Category
consumer_product
Product Description
This recall involves prescription drugs Nurtec ODT 75 mg orally disintegrating tablets sold in cartons containing one bl
Context & Analysis
This is a unclassified recall.
This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Biohaven Pharmaceuticals Inc., of New Haven, Conn. has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Biohaven Pharmaceuticals Inc., of New Haven, Conn.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Biohaven Pharmaceuticals Inc., of New Haven, Conn. have FDA actions?
Biohaven Pharmaceuticals Inc., of New Haven, Conn. has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9565" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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