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HHP Medication Safety Watch: October 2024
This list contains selected items from the full FDA list of recalls, withdrawals, and alerts for medicines and certain health products. We've provided links to FDA information for each product and its maker. Unless otherwise noted, these actions apply only to the specific brand name of the product listed. Talk to your healthcare provider before stopping or changing any medicines or treatments that they have recommended for you.
Over-the-counter products and medicines
Dietary supplement recalled due to contamination with three drugs
- AK Forte, 400 mg tablets (maker: C&A Naturistics)
Comment: All lots of this product were recalled by its maker after FDA testing found contamination with diclofenac, dexamethasone, and methocarbamol. Diclofenac is an anti-inflammatory medicine in the same family as ibuprofen. Its side effects include stomach upset, stomach ulcers, and kidney injury. Dexamethasone is a steroid medicine that can cause serious side effects, including increased blood sugar and blood pressure and reduced ability to fight infections. Methocarbamol is a muscle relaxant that may cause sedation, low blood pressure, and dizziness.
AK Forte is sold as a treatment for joint pain.
Skin spray warning due to contamination with steroids
- Skin-Cap aerosol spray products (distributor: Chemigroup France)
Comment: The FDA warns people not to use any Skin-Cap aerosol spray product after testing revealed contamination with a high-potency steroid.
Long-term use of topical steroids may cause significant side effects, including thinning skin, higher blood pressure and blood sugar, weakening of bones (osteoporosis), and reduced adrenal gland function.
People using this product should ask their doctor about the best course of action. Abruptly stopping steroids is not safe and can cause significant side effects, including fatigue, muscle weakness, low blood sugar, and low blood pressure.
This product is sold as a treatment for psoriasis, seborrhea, eczema, and other skin conditions.
Prescription medicines
Duloxetine recalled due to cancer-causing contaminant
- Duloxetine (Cymbalta), 20 mg delayed-release capsules (maker: maker: Towa Pharmaceutical; distributor: Breckenridge Pharmaceutical, Inc.)
Comment: The makers of this medicine have recalled more than 7,000 bottles after testing revealed higher than allowed levels of a nitrosamine, called N-nitroso duloxetine. While nitrosamines are found at low levels in water and foods, exposure to higher than acceptable levels over time may increase cancer risk.
Duloxetine is prescribed for depression, anxiety, and certain conditions causing chronic pain.
Read additional issues of HHP Medication Safety Watch
Disclaimer:
As a service to our readers, Harvard Health Publishing provides access to our library of archived content. Please note the date of last review or update on all articles.
No content on this site, regardless of date, should ever be used as a substitute for direct medical advice from your doctor or other qualified clinician.

Extreme heat endangers older adults: What to know and do

Want to cool down? 14 ideas to try

What is a PSA test and how is it used?

Blood sugar–friendly fruits if you have diabetes

Gratitude enhances health, brings happiness — and may even lengthen lives

Respiratory health harms often follow flooding: Taking these steps can help

Could tea tree oil help treat acne or athlete’s foot?

Hemoglobin A1c (HbA1c): What to know if you have diabetes or prediabetes or are at risk for these conditions

What could be causing your blurry vision?

Avocado nutrition: Health benefits and easy recipes
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