FDA Issues Recall for Blood Pressure Medications for Oxycodone Detection

In addition to taking blood pressure medications at a safe range, many Americans also undertake a number of lifestyle adjustments to regulate their blood pressure levels. 

The Cleveland Clinic stated that medications can help avoid heart failure, kidney disease, a cardiac arrest, or a stroke, which are serious health concerns to take into account if you belong to the 116 million individuals with high blood pressure. 

Nevertheless, despite the fact that these drugs are meant to benefit your health, one type is currently being recalled because it contains oxycodone hydrochloride. 

Continue reading to learn how to proceed if you have these blood pressure medications at home. 

1. An Oxycodone Tablet Was Found Amid the Packaging of Blood Pressure Drugs

One batch of Betaxolol Tablets are being voluntarily recalled by KVK-Tech, Inc., as per an FDA recall. The betaxolol pills are described on the notice as being white, spherical, and bearing the writing “K13” on one surface.

The tablets were delivered to multiple retail pharmacy locations all over the country in white cans and bottles that held 100 pills apiece. Because the batch contained oxycodone hydrochloride, a common opioid drug of abuse, the batch was withdrawn as a means of prevention.

The company discovered one 5mg oxycodone hydrochloride capsule on the packing line during line approval, which is the method for making sure equipment is devoid of contaminants, after the betaxolol batch was handled, according to the press release.

2. Severe Health Concerns Emerge from Taking an Opioid

According to the FDA recall notice, there are significant health hazards for various patient populations if more oxycodone pills were inadvertently packaged with or in place of regular medications that regulate blood pressure levels.

The package insert for betaxolol contains a warning about heart rate slowing in older individuals, which is likely to be made worse by opioid use disorder, as stated by the Cleveland Clinic. Also, some patients who receive modest doses of betaxolol may already have impaired lung function and heart rate, which is likely to be made worse by an opiate.

However, those who accidentally ingest a narcotic can suffer consequences, including those who have or are at risk for opioid use disorder, newborns, kids, and elderly people. This is particularly true if a sizable quantity of oxycodone tablets has been added to a bottle that has betaxolol written on it.

3. Stop Taking These Drugs Immediately

The FDA observes that there are only slight visual variations among betaxolol and oxycodone hydrochloride pills. In fact, the FDA claims that you presumably would not notice any distinction even if you regularly took 10-milligram betaxolol tablets.

If you purchased recalled pills from the retail pharmacy, stop using them right away, and send them back to the manufacturer right away even if the company has not heard of any accusations of foreign tablets being found in boxes of betaxolol capsules. 

According to the announcement, the corporation will pay you back for the price of the drug. Make an appointment with your doctor or other healthcare practitioner if you suffer any problems with your blood pressure levels’ drugs, as advised in the press release.  

4. The Manufacturer Is Vigorously Alerting the Public

According to an FDA press release, the manufacturer alerted suppliers and clients of the recall through electronic mail and FedEx express delivery. The business is currently setting up the return of the recalled batch’s goods.

The business also mentioned that a few bottles might have ended up at a retail pharmacy here and there. Contact the business with details concerning the recall.