Betaxolol Tablets
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
Yes — there is an active recall. 1 ongoing FDA recall mention Betaxolol (3 total). Check the affected lots below.
Most common reason: cGMP deviation (1 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Betaxolol. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
CGMP Deviations:
Microbial Contamination of Sterile Products: Confirmed sterility failure identified during stability testing at the 12-month time point.
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