2,715 recalls tagged with “immediate action”.
Yetonamr recalled Pull String Teething Toys on January 22, 2026, due to choking risks. The toys violate safety standards with silicone strings that can obstruct breathing. Consumers must stop using the toys immediately and seek refunds.
Topkay recalled torch lighters on January 22, 2026, due to serious fire and burn hazards. The lighters lack required child-resistant features, posing risks to consumers. The recall affects lighters sold on Amazon by Xiyude.
Vndueey recalled its Magnetic Men toy sets on January 22, 2026, due to ingestion hazards. The sets contain loose magnets that can pose serious health risks to children. Consumers should immediately stop using the toys and seek a refund.
Gagaku recalled ice cream shop toy playsets on January 22, 2026, due to a magnet ingestion hazard. The toys can pose serious injury or death risks if magnets detach and are swallowed. Consumers should stop using the toys and seek a refund immediately.
Thrasio recalled Angry Orange Enzyme Stain Removers on January 22, 2026. The products may contain the bacteria Pseudomonas aeruginosa, posing serious health risks. Consumers should stop using the product and seek a refund immediately.
Unichem Pharmaceuticals recalled Bisoprolol Fumarate and Hydrochlorothiazide tablets on January 21, 2026. The recall affects tablets that do not meet impurity specifications for N-Nitroso Bisoprolol. Consumers should stop using the product and contact their healthcare provider immediately.
Stryker recalled 5,864 units of the MOLLI 2 surgical markers on January 21, 2026. The recall follows concerns that magnetic surgical tools may dislodge markers during procedures. Healthcare providers and patients must stop using these devices immediately.
STAAR Surgical AG recalled 7 EVO+ Visian TICL VTICM5 lenses after finding a labeling error that listed 12.1 mm length but which are 12.6 mm. The mismatch can cause excessive vault and ocular complications. Physicians and patients should stop using the device immediately and follow manufacturer instructions for recall actions.
Auris Health recalled 173 bronchoscopy devices due to a software malfunction. This issue could lead to improper robotic arm positioning, risking patient safety. The recall affects devices distributed nationwide and in Canada, with the announcement made on January 21, 2026.
Unichem Pharmaceuticals recalled 60,000 bottles of Doxazosin Tablets on January 21, 2026. The tablets were imprinted with the wrong ID, posing a serious risk to consumers. Healthcare providers and users should stop using the product immediately.
Agiliti Health recalled 4,286 Adapt Pumps on January 21, 2026, after identifying a malfunction. The issue prevents the Microclimate Management function from re-engaging following the Autofirm function. This defect poses a risk to patients relying on the device for safe pressure management.
Acme United Corporation recalled Med Nap BZK Antiseptic Towelettes, 100-count, distributed nationwide. The FDA-listed CGMP deviations raise concerns about manufacturing quality and product safety. Consumers and healthcare providers should stop using the product and follow the recall letter for guidance.
Dynarex recalled 1,000-pack BZK Antiseptic Towelettes nationwide after CGMP Deviations were identified. The product contains benzalkonium chloride 0.13% and carries NDC 67777-245-04. Consumers should stop using this product immediately and await recall notification by letter.
ACME United recalled WP WipesPlus Hand Sanitizing Wipes, 100-count, sold nationwide, after CGMP deviations were identified. The recall is classified as Class II. Consumers should stop using the product immediately and await guidance from ACME United. The NDC is 67151-727-01.
Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.
ACME United Corporation recalled 212,607,900 First Aid Only BZK Antiseptic Towelettes sold nationwide. The recall cites CGMP deviations in manufacturing. Consumers should stop using the product immediately and contact ACME United Corporation for guidance.
ACME United Corporation recalled BZK Antiseptic Towelettes sold for Food Service Resources nationwide after CGMP deviations were found. The recall is Class II and high risk. Consumers and healthcare providers should stop using this product immediately and follow recall guidance.
ACME United Corporation recalled Medi-First Antiseptic Wipes sold nationwide in the United States. The recall cites CGMP deviations that could affect product quality. Consumers and healthcare providers should stop using the wipes immediately and contact ACME United Corporation or a healthcare provider for guidance.
ACME UNITED recalled Max Packaging Antibacterial Towelette nationwide in the United States after CGMP deviations were identified. Manufacturing quality deviations prompted the recall, classified as Class II and labeled as high hazard. Stop using the product immediately and contact ACME UNITED CORPORATION or your healthcare provider for guidance.
ACME United Corporation is recalling Savannah Antibacterial Towelettes nationwide after CGMP deviations in manufacturing. The deviations may affect product quality and safety. Stop using the product immediately and contact ACME United or your healthcare provider for guidance.