233 recalls tagged with “choking hazard”.
In My Jammers recalls children's button-up flare pajama sets sold online after the company violated mandatory flammability standards. The recall, active as of Sept. 11, 2025, involves sets in multiple prints and sizes. Parents should stop using them and seek a full refund or store credit.
Shierdu recalled a 28-piece wooden cactus toy set sold on Amazon by Yiwu Shiyi Trading after reports the parts pose a choking hazard for children under three. The recall cites violation of the Small Parts Ban. Parents should stop using the product and contact the supplier for a full refund.
Harris Teeter recalls 295 units of Asiago Texas Toast distributed in eight states after discovering undeclared milk. The allergen milk was not listed in the ingredient statement. Consumers with milk allergies should avoid the product and seek refunds or replacements.
Olympus Corporation of the Americas recalls 8,587 bronchovideoscope units worldwide, including 4,297 in the US and 4,290 outside. The recall centers on updated IFU language for safe use with laser, argon plasma coagulation and high-frequency therapy equipment. Stop using the device immediately and follow manufacturer instructions for remediation.
Olympus Corporation of the Americas recalls its BF-P150 bronchoscope after updates to the instruction for use. The recall covers 1,019 units outside the U.S. Distribution was nationwide in the U.S. The agency classifies this as a high-hazard issue.
Gina Marie Bakery LLC recalled 172 cases of Toasted Almond & Cherry Biscotti after the FDA flagged undeclared Red 40. The recall is classified as high hazard. Consumers should avoid the product and contact the company for refunds or replacements.
Gina Marie Bakery LLC recalled 172 cases of Italian Sesame Cookies after discovering undeclared sesame and artificial colorings. The recall began with CT state actions and was notified to FDA on 09/10/2025 with customer notification on 09/11/2025. Consumers should not eat these cookies and should seek refunds or replacements.
Gina Marie Bakery LLC recalled 3,440 Vanilla Cookies with Raspberry Peach Jam distributed in Connecticut after undeclared Red 3 and Blue 1 were detected. The recall was announced by state authorities and shared with FDA. Consumers should not eat the product and should contact Gina Marie Bakery LLC for refunds or replacements.
Lee K of NY Inc. recalls 43 units of PINOCCHIO CATERING Aged Kimchi Mackerel sold in New York and New Jersey for undeclared milk and shrimp. The recall is Class I with a high hazard. Consumers should not consume the product and should contact the company for refunds or replacements.
Chetak New York announced a recall of 3,509,532 bags of Deep-brand Select Tindora on September 5, 2025. The product tested positive for Salmonella, a serious foodborne pathogen. Consumers should not consume the product and seek a refund or replacement immediately.
Zydus Pharmaceuticals USA Inc. recalls Entecavir tablets after FDA enforcement reports impurity/degradation failures. The recall affects 4,440 bottles distributed nationwide. Providers and patients should stop use and seek guidance from a healthcare professional.
Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane imaging systems worldwide, including 102 in the United States. The recall cites deterioration of internal components that could disable motorized movements. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.
Endico Potatoes Inc. recalled 335 cases of Endico brand PEAS & CARROTS distributed to seven states after authorities flagged Listeria monocytogenes. The product should not be eaten. Consumers should contact Endico Potatoes for refund or replacement information. The recall was active as of Sept. 3, 2025.
Chlorpromazine Hydrochloride Tablets, 200 mg, 100-count bottle, manufactured by Zydus Lifesciences Ltd. and distributed by Northstar Rx LLC, are under recall nationwide in the United States. The CGMP deviation involves elevated levels of N-Nitroso Desmethyl Chlorpromazine. Consumers should stop use and contact their healthcare provider.
The FDA confirms a nationwide recall of Zydus Lifesciences Chlorpromazine Hydrochloride tablets 200 mg (NDC 70710-1133-1) distributed by Zydus Pharmaceuticals USA. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above acceptable intake. Consumers and healthcare providers should stop using the product immediately and contact the distributor for guidance.
Philips Medical Systems Nederland B.V. recalls 53 units of the Allura Xper CV20 system due to a BIOS battery that may deplete faster than designed. The recall affects units distributed worldwide, including the US and many other countries. The failure prevents system startup with no prior warning messages.
Granules Pharmaceuticals Inc. recalls 3,384 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, 100 capsules per bottle, NDC 70010-029-01, Lot GPC250158A, Exp 06-22-2027. The recall concerns failed impurities/degradation specifications. Healthcare providers and consumers should stop using the
CT New Energy Technology recalls CT-ENERGY nc-02 lithium coin battery chargers sold with four rechargeable 2032 batteries and a USB cable. The recall cites potential for serious injury or death from ingested button cells. Consumers should stop using the charger and contact CT New Energy for a full refund, repair, or replacement kit.
Granules Pharmaceuticals recalled 9,917 bottles of mixed-salts amphetamine extended-release capsules nationwide. The recall was issued August 28, 2025 and remains active. The FDA cited failed impurities/degradation specifications as the reason. Healthcare providers and consumers should stop using the product immediately and contact Granules Pharmaceuticals for guidance.
Party Favors recalled four models of lite-up torches and laser pointers due to risk of serious injury or death from swallowed button cell batteries. Imported by MTC Trading. Consumers should stop using the products and seek a full refund.