- Cosmetics
by FDA on May 14, 2025 at 3:55 pmConsumer articles about cosmetics.
- Radiation-Emitting Productsby FDA on May 14, 2025 at 4:01 pm
From medical X-ray scanners used to see inside the body to surgical lasers used for cosmetic purposes or to improve eyesight, FDA ensures the safety and effectiveness of a wide range or products that emit radiation. To learn more, read these Consumer Updates.
- FDA 101: Product Recallsby FDA on June 11, 2025 at 7:03 pm
Recalls are typically voluntary actions taken by a company to remove or correct products on the market that violate U.S. Food and Drug Administration laws and regulations. Recalls may be initiated proactively by a company, at FDA request, or ordered under statutory authority.
- Safely Using Hand Sanitizerby FDA on August 6, 2025 at 7:37 pm
You can help stop the spread of infectious diseases by washing your hands with soap and water for 20 seconds every time. If soap and water are not available, alcohol-based hand sanitizers can be used if they contain at least 60% alcohol and are used properly.
- Olympus Announces Voluntary Corrective Action for the Single-Use Ligating Device
by FDA on December 18, 2025 at 5:00 amCenter Valley, Pa., (December 5, 2025)-Olympus Corporation today announced a voluntary medical device corrective action for its Single-Use Ligating Device (“Polyloop”) following identification of a potential safety issue.
- StuffbyNainax LLC Issues Voluntary Nationwide Recall of MR.7 SUPER 700000 Dietary Supplement Due to the Presence of Undeclared Sildenafil and Tadalafilby FDA on December 16, 2025 at 5:00 am
Huntsville, Texas — StuffbyNainax LLC is voluntarily recalling all lots of MR.7 SUPER 700000 capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil and tadalafil, which are active ingredients in FDA-approved prescription drugs used to treat male erectile dys
- MediNatura New Mexico, Inc. Expands Voluntary Nationwide Recall of ReBoost Nasal Spray and to include ClearLife Allergy Nasal Spray Due to Microbial Contaminationby FDA on December 16, 2025 at 5:00 am
FOR IMMEDIATE RELEASE – December 16, 2025 – Albuquerque, New Mexico, MediNatura New Mexico, Inc. is voluntarily recalling all lots of ReBoost Nasal Spray to the consumer level. The product has been found to contain yeast/mold and microbial contamination with one species identified as Achromobacter,
- Early Alert: Anesthesia System Issue from GE HealthCareby FDA on December 10, 2025 at 5:00 am
GE HealthCare issues updated use instructions for certain Carestation 600 and 700 series Anesthesia Systems
- MediNatura New Mexico, Inc. Issues Voluntary Nationwide Recall of ReBoost Nasal Spray Due to Microbial Contaminationby FDA on December 10, 2025 at 5:00 am
FOR IMMEDIATE RELEASE – December 10, 2025 – Albuquerque, New Mexico, MediNatura New Mexico, Inc. is voluntarily recalling one lot of ReBoost Nasal Spray to the consumer level. The product has been found to contain yeast/mold and microbial contamination with one species identified as Achromobacter, a