Betaxolol Tablets have been recalled due to contamination with o xycodone HCl tablets. Betaxolol is a medication to control blood pressure....
Betaxolol Tablets have been recalled due to contamination with oxycodone HCl tablets.
Betaxolol is a medication to control blood pressure.
Oycodone HCl is an opioid medication used to relieve moderate to severe pain.
Risk: Betaxolol may slow heart rate in elderly patients, which can be exacerbated by opioid medications.
Betaxolol HCl Tablets are packaged in 50 CC White High-Density Polyethylene (HDPE) bottles, 100 Tablets and 10702-013-01. The affected Betaxolol Tablets, USP 10 mg lot 17853A has labeled expiration as June 2027. The product can be identified by using the images of tablets and labels provided below.
Consumers with questions regarding this recall can contact KVK-Tech Inc., at (215) 579-1842 Ext: 6002 Monday – Friday, 8:00 am – 6:00 pm EST or by email at customerservice@kvktech.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Complete and submit the report online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: Download from www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
