Extra-Strength Unaspirin caplet (Acetaminophen 500 mg) Bulk Container, ULTRAtab Laboratories, Inc...
FDA Recall #D-0535-2022 — Class II — January 26, 2022
Product Description
Extra-Strength Unaspirin caplet (Acetaminophen 500 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62959-207-00
Reason for Recall
CGMP Deviations
Recalling Firm
ULTRAtab Laboratories, Inc. — Highland, NY
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
6,215,512 tablets
Distribution
Bulk product was distributed to 3 distributors who may have distributed finished product.
Code Information
Product Codes: L207L Bulk Lots: 18K111, 19E104, 19F050
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated
What Should You Do?
Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.