2,142 recalls tagged with “cpsc regulated”.
Volkswagen Group of America is recalling 2025 ID. BUZZ vehicles due to a third-row seating flaw. The rear bench is wide enough for three passengers but equipped with only two seat belts. Dealers will install trim to adjust the width at no cost, and owner letters were mailed June 20, 2025. Contact VW at 1-800-893-5298 for details and recall 72LC.
Cook Medical recalled 5,080 Spectrum Central Venous Catheter Sets worldwide after labeling that indicated expiration dates beyond the products' true shelf life. The recall alerts patients and healthcare providers to stop using affected lots and follow manufacturer instructions.
Cook Medical recalled 15 CTO-6 Micro Wire Guides sold worldwide after labeling errors extended expiration dates beyond true shelf life. The devices carry Reference Part Number CMW-14-190-6G and Order Number G50786. Healthcare providers were notified to stop use immediately until further instructions.
Cook Medical recalled the Thal-Quick Chest Tube Tray, reference part number C-TQTSY-3200, Order G07242, due to expiration dates that exceed true shelf life. The recall is active and worldwide. The hazard is labeling that misstates shelf life. Patients and healthcare providers should stop using the affected devices immediately and follow Cook’s recall instructions.
Tornier recalls 233 surgical parts nationwide in the United States. The items were mislabelled as Tornier HRS Max products. These parts fit the Tornier HRS system only and are incompatible with the Tornier HRS Max system. Clinicians and patients should stop using the affected parts and follow recall instructions.
Cook Medical recalled 916 units of the Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set worldwide after discovering expiration dates exceeded true shelf life. The recall affects multiple reference part numbers and order numbers. Healthcare providers should stop using the device immediately and follow Cook’s instructions for recall notification.
Cook Incorporated recalled 20 units of its Multipurpose Drainage Catheter reference ULT8.5-38-25-P-CLMS-8-RH-FS distributed worldwide. The recall cites expiration dates that exceed the product’s true shelf life. Healthcare providers and patients should stop using the affected devices immediately.
Cook Incorporated recalls 484 Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Sets due to expiration date labeling that exceeds true shelf life. The recall is active and distributed worldwide. Health care providers must stop use and follow recall instructions.
Cook Medical recalled 70 NCompass nitinol stone extractors worldwide after labeling showed expiration dates that exceed their true shelf life. The recall affects lots labeled C-NTSE-2.4-115-NC3 (G36250) and C-NTSE-2.4-115-NCT4 (G36251). The company classifies the action as Class II and says the issue could affect patient safety.
Cook Medical recalled 318 Wayne Pneumothorax Trays after labels showed expiration dates beyond true shelf life. The devices were distributed worldwide. Patients and healthcare providers should stop using these devices immediately and follow recall instructions from Cook Incorporated.
Cook Medical recalled 1,872 units of Spectrum Central Venous Catheter Trays worldwide due to expiration dates labeling that exceed true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions."
Cook Medical issued a global recall of 95 units of the Cook Staged Extubation Set due to expiration dates that exceed true shelf life. The affected lots carry Reference Part Number C-CAE-14.0-83-EXTU and Order Number G24073. The recall is classified as HIGH hazard. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Cook Incorporated.
Cook Medical recalled 49 units of the Strange Bile Duct Stone Exploration Set due to labels showing expiration dates beyond shelf life. The recall is worldwide and active as of March 5, 2026. Healthcare providers were advised to stop use and follow recall instructions.
Toyota recalls 2022-2025 Tundra and Tundra Hybrid vehicles because moisture in the reverse light assemblies can cause light failure. Dealers will replace both reverse light assemblies and repair wire harnesses. Owner letters were mailed September 11, 2025. Contact Toyota at 1-800-331-4331 for recall 24TB06 and 24TA06.
Cubimana recalled its Island Storm 3 In 1 Building Sets on March 5, 2026, due to a risk of serious injury or death from battery ingestion. The sets violate safety standards as they contain accessible button cell batteries. Consumers should stop using and return the product immediately for a full refund.
Unique Brands Com recalled Forever 21 Kids Disney Mickey Mouse Pajama Pants on March 5, 2026. The pants pose a significant burn hazard due to flammability standards violations. Parents should stop using them immediately and seek a refund.
Koven Technology recalled 34 BiDop 3 Pocket Dopplers with BT2M20S8C fetal probes nationwide after regulators found the fetal indication on the labeling was not cleared under 510(k). The defect is labeling that misrepresents fetal use. Healthcare providers and patients should stop using the devices and follow recall instructions from the manufacturer.
Ajinomoto Foods North America recalls Ajinomoto Golden Tiger Vegetable Fried Rice sold at multiple retailers nationwide. Glass fragments measuring 1-3 cm long and 2-4 mm wide have been found in frozen rice. Consumers should not eat the product and should contact Ajinomoto for refunds or replacements.
Philips Medical Systems Nederland recalled 5,167 Azurion 7 M20 X-ray imaging systems sold to healthcare facilities in the U.S. and internationally. The wired foot switch can fail to initiate imaging or produce intermittent imaging. Hospitals and clinics should stop using the device and follow recall instructions from Philips, with notification by letter to affected parties.
Philips Medical Systems Nederland B.V. recalled 5,084 ALLURA Xper FD20 imaging systems sold nationwide and internationally after finding that the wired foot switch may fail to initiate X-ray imaging or perform intermittently. The defect can delay or interrupt imaging during patient care. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.