KVK-Tech, Inc. 2023-10-25 Health critical FDA
Health · FDA · Recall #FDA-D-0049-2024
Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown,… Recall
Issued October 25, 2023 · KVK-Tech, Inc.
In October 2023, KVK-Tech, Inc. recalled the Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown,…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
What you should do
- 1 Stop using Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact KVK-Tech, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- KVK-Tech, Inc.
- Category
- Health
- Recall date
- October 25, 2023
- Units affected
- Not reported
- Sold at
- Nationwide in the USA and PR
- Recall number
- FDA-D-0049-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- KVK-Tech, Inc. has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.