1,882 product recalls found in this category. Browse through all safety alerts and stay informed.
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This category has a significant number of recalls. Please check regularly for updates.
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.
Cook Medical recalled 75 CTO-18 Micro Wire Guide devices distributed worldwide. The recall cites expiration date labeling that exceeds the true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions.
Tomum recalled its Minoxidil Hair Growth Treatment on March 5, 2026, due to serious poisoning risks to children. The product lacks required child-resistant packaging, increasing the risk of ingestion. Consumers should stop using the product immediately and contact the company for a safe replacement.
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.
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.
Philips Medical Systems Nederland B.V. recalls 2 ALLURA Xper FD10 OR Tables after reports that X-ray imaging may not start or may delay when using the wired foot switch. The defect could affect patients during imaging procedures. Healthcare providers should stop using the device and follow recall instructions from the manufacturer.
KC Pharmaceuticals recalled 182,424 Sterile Eye Drops AC bottles sold nationwide under multiple brands including Quality Choice Eye Drops Irritation Relief and Goodsense Ultra Lubricant Eye Drops. The recall cites a lack of assurance of sterility. Consumers should stop using the product immediately and contact KC Pharmaceuticals for guidance.
Philips recalled 112 ALLURA Xper FD10/10 imaging systems nationwide in the United States and internationally after reports that X-ray imaging may not start or may intermittently stop when using the wired foot switch. The defect affects system codes 722005, 722011, and 722027. Healthcare providers should stop using the devices and follow Philips recall instructions.
Philips Medical Systems Nederland B.V. recalled 345 Azurion 5 M12 X-ray systems distributed worldwide after reports that X-ray imaging may not start or may run intermittently when using the wired foot switch. The defect could affect imaging during patient care. Hospitals should stop using the device immediately and follow the recall instructions in the notification letter.
Oxoid recalled 2 Microbact 12L Kit 20 Tests MB1128A lot 4494873 distributed nationwide in the United States, including Georgia and California. The kit may identify the wrong organism due to inconclusive color reactions in wells. Laboratories should stop using the kit immediately and follow recall instructions from Oxoid.
Philips Medical Systems Nederland B.V. recalls 1,523 Azurion 7 B20 interventional X-ray systems used by hospitals nationwide after possible failure to initiate X-ray imaging. The defect affects whether imaging starts when using the wired foot switch. Hospitals should stop using the device and follow Philips recall instructions immediately.
Philips Medical Systems Nederland B.V. recalls 4 units of the Allura Xper FD20 Biplane OR Table after identifying intermittent or failed X-ray initiation when using the wired foot switch. The recall covers System Codes 722020 and 722025. Healthcare facilities were notified by letter. Stop using the affected devices and follow Philips instructions.
Philips recalls 298 Azurion 3 M12 X-ray imaging systems used by healthcare providers worldwide. The issue is that X-ray imaging may not start or may be intermittent when using the wired foot switch. Stop using the affected devices immediately and follow recall instructions from Philips.
Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.
Philips Medical Systems Nederland B.V. recalled 920 Azurion 5 M20 imaging systems worldwide, including 168 in the United States. The recall cites a defect in which X-ray imaging may not start or may begin intermittently when using the wired foot switch. Healthcare providers should stop using the device immediately and await instructions from Philips.
Philips Medical Systems Nederland B.V. recalls 111 Allura Xper FD20/20 imaging systems with System Code 722038. The recall covers 31 units in the United States and 80 abroad. The defect may prevent X-ray imaging from starting or cause intermittent imaging when using the wired foot switch. Stop using the device immediately and follow recall instructions from Philips or your healthcare provider.