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 recalls have press releases or are posted on this page. See Additional information about recalls for a more complete listing.
The Recalls, Market Withdrawals & Safety Alerts are available on FDA’s website for three years before being archived. To search archived content, visit Search FDA Archive and input the name of the product and/or company name in the Search terms box as well as the year to get the most inclusive search results. To scroll through archived Recalls, Market Withdrawals & Safety Alerts content by year, see the Recall and Safety Alerts Archive.
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| Date | Brand Name(s) | Product Description | Product Type | Recall Reason Description | Company Name | Terminated Recall | Excerpt |
|---|---|---|---|---|---|---|---|
| Fresenius Kabi | Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL | Drugs | Due to a label mix-up | Fresenius Kabi | … labeled as Morphine 2 mg/1 mL, may contain a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL. This recall is being conducted … the use of this product may be reported to Fresenius Kabi Medical Affairs or Vigilance departments at 1-800-551-7176, … devices, disposables, and world-leading blood collection systems; and intravenous generic drugs and fluids that … | ||
| Medtronic | MiniMed™ 600 series or 700 series insulin pumps | Medical Devices | Device & Drug Safety - Defect | Medtronic plc | … battery status and to contact Medtronic if they observe changes in the battery life of their pump. Medtronic began … or diabetic ketoacidosis (DKA), potentially requiring medical intervention. Most recently, Medtronic has received … robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, … |