Recalls, Market Withdrawals, & Safety Alerts | FDA
Recalls, Market Withdrawals, & Safety Alerts. The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Not all ...
Voluntary Recall Notifying Medtronic Insulin Pump Users of …
6 days ago · When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company. Read ...
Antidepressant recall: FDA upgrades medication risk class to 2nd ...
2 days ago · The U.S. Food and Drug Administration updated the risk level of an antidepressant recall to the second-highest level due to the product containing high levels of a cancer-causing chemical.
Insulin Pump Recall: Medtronic Notifies Users of MiniMed 600 …
6 days ago · Medical Device Recall Database Class 1 Device Recall MiniMed 620G, 630G (OUS only), 640G, and 740 Insulin Pumps. (fda.gov) Class 1 Device Recall Medtronic MiniMed 630G and 700G Insulin Pumps (fda.gov)
FDA announces recall of heart pumps linked to deaths and injuries
Apr 16, 2024 · A pair of heart devices linked to hundreds of injuries and at least 14 deaths has received the FDA's most serious recall, the agency announced Monday.
Blood pressure medicine recalled due to potential cancer risk: FDA
Oct 27, 2022 · A pharmaceutical company is recalling a blood pressure medication due to a potential cancer risk, the FDA announced this week. Aurobindo Pharma USA is recalling two lots of quinapril and...
FDA says 561 deaths tied to recalled Philips sleep apnea machines
Feb 4, 2024 · The Food and Drug Administration says 561 deaths have been reported in connection to recalled Philips devices to treat obstructive sleep apnea and other breathing disorders.
Over 400 ready-to-eat foods are recalled over listeria ... - NPR
Feb 7, 2023 · More than 400 food products — including ready-to-eat sandwiches, salads, yogurts and wraps — were recalled due to possible listeria contamination, the Food and Drug Administration announced ...
UPDATE: Do Not Use Cue Health’s COVID-19 Tests
Oct 16, 2024 · The U.S. Food and Drug Administration (FDA) is warning home test users, caregivers, and health care providers not to use Cue Health’s COVID-19 Tests for Home and Over-the-Counter (OTC) Use and ...
FDA warns eye drops may cause infection. Here's a list of 27 ... - CBS News
Nov 2, 2023 · FDA urged recall of eye drops exposed to insanitary conditions at factory, but products listed may still be available for sale and pose risk of infection, agency says.
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