Guanfacine Extended-Release Tablets 2 mg,100-count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326, NDC 60505-3928-1, UPC 3 60505 39281 0
Reported: April 14, 2021 Initiated: March 31, 2021 #D-0324-2021
Product Description
Guanfacine Extended-Release Tablets 2 mg,100-count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326, NDC 60505-3928-1, UPC 3 60505 39281 0
Reason for Recall
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
Details
- Recalling Firm
- Apotex Corp.
- Units Affected
- 55620 bottles
- Distribution
- Nationwide within the United States
- Location
- Weston, FL
Frequently Asked Questions
What product was recalled? ▼
Guanfacine Extended-Release Tablets 2 mg,100-count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326, NDC 60505-3928-1, UPC 3 60505 39281 0. Recalled by Apotex Corp.. Units affected: 55620 bottles.
Why was this product recalled? ▼
Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 14, 2021. Severity: Moderate. Recall number: D-0324-2021.
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