233 recalls tagged with “choking hazard”.
Boston Scientific recalled 156 units of the Extractor Pro RX Retrieval Balloon Catheter nationwide in the United States after labeling inconsistencies were found. The label misstates whether the skive hole is above or below the balloon. The recall is active as of 2025. Stop using the device immediately and follow manufacturer instructions.
Air Vent recalled electric motors used in gable- and roof-mounted attic fans sold from August 2003 through December 2013. The recall covers five model numbers and centers on a safety cutoff that may short and ignite. Owners should stop using recalled motors and contact Air Vent for a full refund.
Siemens Medical Solutions USA recalled 30 MAGNETOM Skyra fit MRI units worldwide after identifying an ice blockage in the magnet venting system. The defect could prevent helium venting during a quench, causing pressure buildup that may rupture the helium containment and leak into the scanning room. Hospitals should stop using the affected devices immediately and follow the manufacturer’s recall,咨询
Middlefield Original Cheese Cooperative recalled 364.125 cases of shredded Mozzarella/Provolone cheese sold in Ohio, Pennsylvania, Wisconsin, and Texas. The recall is due to potential contamination with Listeria monocytogenes. Consumers who purchased this product should not consume it and should contact the cooperative for refund or replacement information.
Middlefield Original Cheese Cooperative recalls 7,455 pounds of Original Swiss Cheese distributed in Ohio, Pennsylvania, Wisconsin and Texas after potential Listeria monocytogenes contamination. The recall affects 5‑lb loaves and 2‑lb deli bags in various packaging. Consumers should not eat this cheese and should contact the cooperative for refund or replacement information.
A high-severity recall covers chlorpromazine hydrochloride tablets distributed nationwide by American Health Packaging. A foreign substance linked to a polyester coil packaging component was detected at the manufacturing site. No tablets were contaminated. Stop using the product and contact the distributor for guidance.
FDA enforcement lists 230 bottles of Cyclobenzaprine labeled incorrectly as Meloxicam. The labeling error was detected in a nationwide recall. Health professionals and patients should stop using the mislabeled bottles immediately. Contact Unichem Pharmaceuticals USA or a clinician for guidance.
CooperVision recalled one lot of Voyant 1-Day Premium Toric contact lenses sold nationwide in the United States after an invalid sterilization cycle was detected. The recall affects 90 units distributed in Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the lenses immediately and contact their eye care professional for guidance.
Ford is recalling certain 2025-2026 F-550 SD, F-450 SD, F-350 SD, F-250 SD, and 2025 F-150 vehicles because the instrument panel may fail at startup. The recall covers 2025-2026 models. Ford will provide an IPC software update via dealer service or OTA at no cost. Owner letters were mailed September 5, 2025. Contact Ford customer service at 1-866-436-7332. Recall number 25S88.
FDA-listed recall covers 49,275 tubes sold nationwide. Ultra Violette Velvet Screen Blurring Mineral Skinscreen distributed by Grace & Fire USA Inc. Tested SPF results ranged from 4 to 64. Consumers should stop using the product immediately and contact Grace & Fire USA for guidance.
Taylor Farms Retail issued a Class I recall for 8,284 salad kits after undeclared sesame and soy allergens were found inside a dressing packet. The recall covers products labeled under Taylor FARMS Honey Balsamic Salad Kit sold across 19 states. Consumers should not eat the product and should seek refunds or replacements from Taylor Farms Retail.
Mercedes-Benz USA recalls 2025 GLC 350E 4MATIC and related EQE/GLC models due to a loose steering coupling bolt. The defect may loosen the steering rack, risking loss of control. Dealers will tighten bolts at no charge. MBUSA notified owners on Oct 6, 2025.
Boston Scientific recalled 28,911 pacemakers worldwide due to a software flaw in Safety Architecture that could prevent Safety Mode when battery impedance is high. The recall covers ACCOLADE family devices and VISIONIST and VALITUDE CRT-Ps. Patients should stop using the device immediately and follow the recall letter instructions.
Toto Foods recalled 120,180 units of Toto S'Mores Ooey Gooey Cookie sold to 6 retailers nationwide after labeling conflicts regarding soy content. The defect involves conflicting statements on whether the product contains soy. Consumers should avoid consumption and seek refund or replacement from Toto Foods.
Amneal Pharmaceuticals products containing chlorpromazine hydrochloride are recalled nationwide after the FDA-linked notice identifies a foreign substance in packaging material. No tablets were contaminated. The recall was issued August 18, 2025 and updated September 10, 2025. Consumers and healthcare providers should stop using the affected lots immediately and contact Amneal for guidance.
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.
STWUQIKONG recalled a three-tier spiral tower toy sold on Shein because of a choking hazard. The recall was announced on August 14, 2025. The toy includes three yellow balls and is designed for children under three, violating the small-ball ban. Stop using the product immediately and email STWUQIKONG_RECALL@hotmail.com to receive a full refund.
Fresh & Ready Foods recalled 233 units of Tuscan Artichoke and Mozzarella Salad distributed to 15 California locations after undeclared wheat and milk allergens were found. The allergen was not declared on the label. Consumers should not eat the product and should contact Fresh & Ready Foods LLC for refunds or replacements via email.
Philips recalled 285 Ingenuity CT systems worldwide, including 728321, 728323 and 728326 models. A ball screw misalignment after a replacement can cause the patient couch to descend to the lowermost position. Hospitals and clinics should stop using the devices and follow Philips recall instructions.
Penner Patient Care recalls 206 US units of the Penner Pacific Bathing Spa after the device lacks a unique device identifier. The recall targets models listed with multiple variations and serial numbers. Consumers should stop using the device immediately and follow manufacturer instructions.