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FDAFDA · Food and drugs·Recall number D-1111-2022

Sumatriptan Succinate Tablets, 100 mg, 9 (1 x 9) Unit-of- use tablets box, Rx only, MFG: Sun Pharmaceuticals, NDC 62756-522-69

Published June 15, 2022 · Recall initiated: April 13, 2022

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

cGMP deviations: Temperature abuse

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
SUMATRIPTAN SUCCINATE
Manufacturer
Mckesson Medical-Surgical Inc. Corporate Office
Distributor
USA nationwide.
UPC
0362756521889
Lot
McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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