FDA drug recalls

Dynarex BZK Antiseptic Towelettes have been recalled because the manufacturer did not follow required quality and safety standards during production. The FDA identified manufacturing practice deviations that could affect product safety or effectiveness. No injuries have been reported.

Green Guard Antiseptic Wipes have been recalled due to manufacturing quality control issues. The FDA found that these wipes did not meet proper manufacturing standards. This affects specific lots distributed nationwide.

Acme United Corporation is recalling certain lots of hand sanitizing wipes due to manufacturing process deviations that do not meet federal standards. The affected wipes contain benzalkonium chloride 0.13% and were distributed nationwide. No injuries have been reported.

WP WipesPlus Hand Sanitizing Wipes (0.13% Benzalkonium Chloride) are being recalled due to manufacturing process deviations that do not meet FDA standards. The affected products were distributed nationwide. No injuries have been reported.

Acme United Corporation is recalling specific lots of Med-Nap Cleansing Towelettes because they were manufactured without following required quality and safety standards. The affected towelettes contain benzalkonium chloride and may not meet safety or sterility requirements.

ACME United Corporation is recalling specific lots of Med-Nap cleansing towelettes (benzalkonium chloride 0.13%) due to manufacturing process deviations. The affected products may not meet quality and safety standards. Two lots are involved: MN15923 (expiring May 2028) and MN25822 (expiring August 2027).

Dynarex Obstetrical Towelettes Cleanser with benzalkonium chloride 0.13% is being recalled because the manufacturer did not follow proper manufacturing practices during production. The affected product was distributed nationwide and may not meet quality and safety standards.

Wipes Plus hand sanitizing wipes have been recalled due to manufacturing quality control problems. The FDA found that the product did not meet required manufacturing standards. No injuries have been reported.

ACME United Corporation is recalling specific lots of BZK Antiseptic Towelettes due to manufacturing quality control problems. The affected towelettes may not meet safety and purity standards required for medical products.

Acme United Corporation is recalling Med Nap BZK Antiseptic Towelettes due to deviations from manufacturing standards that could affect product quality and safety. Multiple lot numbers distributed nationwide are affected. No injuries have been reported.

Medi-First Antiseptic Wipes containing benzalkonium chloride were manufactured with deviations from FDA manufacturing standards. The affected wipes were distributed nationwide and may not meet quality and safety standards.

Savannah Antibacterial Towelettes have been recalled due to deviations from manufacturing quality standards (CGMP). The FDA found issues with how these products were made. No injuries have been reported.

ACME United Corporation is recalling Max Packaging Antibacterial Towelettes (Benzalkonium Chloride 0.13%) due to manufacturing quality deviations. The recall affects specific lots distributed nationwide. No injuries have been reported.

ACME United Corporation is recalling multiple lots of BZK Antiseptic Towelettes (benzalkonium chloride 0.13%) due to manufacturing quality deviations. The towelettes were distributed nationwide under various brand names including Piedmont, Touchpoint, Wellstar Cobb, FSR, and Children's Healthcare of Atlanta labels.

First Aid Only BZK Antiseptic Towelettes have been recalled due to manufacturing quality deviations that do not meet FDA standards. Multiple lot numbers distributed nationwide are affected. No injuries have been reported.

Dukal BZK Antiseptic Towelettes were manufactured without meeting federal quality standards (CGMP deviations). Affected lots were distributed nationwide. No injuries have been reported.

First Aid Only BZK Antiseptic Towelettes (50-count packages) are being recalled because the manufacturer did not follow required quality and safety procedures during production. The recall affects specific lot numbers distributed nationwide. No injuries have been reported.

First Aid Only BZK Antiseptic Towelettes have been recalled due to manufacturing quality control deviations. The FDA determined that certain lots did not meet required manufacturing standards. No injuries have been reported to date.

Teva Pharmaceuticals is recalling specific lots of metoprolol succinate extended-release 200 mg tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication properly in your body. This could affect how well the blood pressure medication works. No injuries have been reported.

Teva Pharmaceuticals is recalling specific batches of Metoprolol Succinate Extended-Release 100 mg tablets because they may not dissolve properly in the body. This means the medication may not work as intended. The recall affects bottles with lot numbers ending in J251 or J252 and expiration dates of 12/2026.

Teva Pharmaceuticals is recalling certain batches of Metoprolol Succinate Extended-Release 50 mg tablets because they may not dissolve properly in the body, which could affect how well the medication works. The affected bottles have specific lot numbers and an expiration date of January 2027. No injuries have been reported.

Teva Pharmaceuticals is recalling specific lots of Metoprolol Succinate Extended-Release 25 mg tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication properly in your body. This could result in the drug not working as intended. No injuries have been reported.

BioGlo Fluorescein Sodium Ophthalmic Strips were not manufactured according to safety standards, raising concerns about sterility. The strips are used by eye care professionals for diagnostic eye exams. All lots distributed nationwide are affected.

Bio Glo Fluorescein Sodium Ophthalmic Strips USP were not manufactured following proper sterility standards. These diagnostic strips, distributed nationwide, may not be sterile and could pose a safety risk if used in the eye.

Wizcure Fluorescein Sodium Ophthalmic Strips (1mg) were not manufactured following proper sterilization standards. These strips are used by eye care professionals to examine the eye surface. Because sterility cannot be assured, there is a potential risk of contamination.

Vista Gonio Eye Lubricant (hypromellose ophthalmic solution) distributed by hi-health was not manufactured following required safety standards, raising concerns about sterility. All lots of this eye drop product are affected. No injuries have been reported to date.

Vista Meibo Tears Propylene Glycol 0.6% eye drops were not manufactured under proper safety conditions, raising concerns about sterility. The FDA issued a recall of all lots distributed nationwide. No injuries have been reported.

Vista Gel Hypromellose eye drops were not manufactured according to FDA safety standards, which means the product may not be sterile. The eye drops were distributed nationwide in the United States. No injuries have been reported.

Vista Tears eye drops were manufactured without proper sterility controls, which means they may not be safe for use in the eye. No injuries have been reported, but the product does not meet FDA safety standards.

Agebox iKids-Growth Night Formula contains ibutamoren, a substance not listed on the label or approved by the FDA for this product. The affected 60-count bottles were sold online through Agebox.com and Amazon.com. No injuries have been reported.