Drug Alerts and Statements

• 2/9/2023 Infants at risk for aluminum toxicity with unapproved potassium phosphates drug product
• 2/2/2023 FDA warns consumers not to purchase or use EzriCare Artificial Tears due to potential contamination
• 11/22/2022 FDA alerts health care professionals of compatibility issues with prefilled glass syringes and certain Luer-activated valve (LAV) connectors
• 11/8/2022 FDA alerts health care professionals of risks to patients exposed to xylazine in illicit drugs
• 8/18/2022 FDA alerts patients, caregivers, and health care providers of cross-compatibility issues with autoinjector devices that are optional for use with glatiramer acetate injection
• 4/29/2022 Bosentan REMS requirements will change June 27, 2022
• 4/26/2022 FDA alerts customers to voluntary recall of compounded drugs due to sterility issues by Drug Depot, LLC, dba APS Pharmacy
• 4/20/2022 FDA warns consumers not to purchase or use Artri and Ortiga products, which may contain hidden drug ingredients
• 3/30/2022 FDA warns patients and health care professionals not to use sterile products from North American Custom Laboratories LLC, dba FarmaKeio Superior Custom Compounding
• 9/17/2021 FDA alerts patients and health care professionals not to use compounded products intended to be sterile from Prescription Labs Inc. dba Greenpark Compounding Pharmacy
• 7/28/2021 FDA alerts patients and health care professionals about clinical trial results showing an increased risk of death associated with Pepaxto (melphalan flufenamide)
• 3/19/2021 FDA advises health care professionals not to use ChloraPrep 3 mL applicators manufactured by BD (Becton, Dickinson and Company)
• 1/15/2021 FDA updates vinca alkaloid labeling for preparation in intravenous infusion bags only
• 12/3/2020 FDA alerts healthcare professionals about the risk of medication errors with tranexamic acid injection resulting in inadvertent intrathecal (spinal) injection
• 9/21/2020 FDA alerts of Perrigo’s voluntary albuterol inhaler recall
• 9/8/2020 FDA alerts health care professionals and oncology clinical investigators about efficacy and potential safety concerns with atezolizumab in combination with paclitaxel for treatment of breast cancer
• 8/14/2020 FDA advises consumers not to use goldenseal root powder distributed by Maison Terre
• 7/2/2020 FDA warns consumers of risk of methanol contamination in certain hand sanitizers
• 6/19/2020 FDA advises consumers not to use hand sanitizer products manufactured by Eskbiochem
• 6/1/2020 FDA alerts patients and health care professionals of Amneal and Impax Laboratories epinephrine auto-injector device malfunctions
• 3/24/2020 FDA alerts patients and health care professionals of EpiPen auto-injector errors related to device malfunctions and user administration
• 10/11/2019 FDA advises consumers not to use Rompe Pecho cough syrup
• 7/23/2019 FDA advises patients not to use Herbal Doctor Remedies’ medicines
• 6/28/2019 FDA warns patients and health care professionals not to use sterile products from Pacifico National Inc., dba AmEx Pharmacy
• 6/25/2019 FDA alerts consumers not to use Kratom NC’s products
• 6/21/2019 FDA alerts patients and healthcare professionals to Infusion Options’ voluntary recall due to quality issues
• 2/12/2019 FDA alerts patients of McDaniel Life-Line’s voluntary recall of Indian Herb
• 2/1/2019 FDA warns compounders not to use glutathione from Letco Medical to compound sterile drugs
• 12/11/2018 FDA alerts consumers not to use two e-liquids sold by HelloCig Electronic Technology
• 12/7/2018 FDA alerts health care professionals and patients not to use drug products intended to be sterile from Promise Pharmacy
• 11/19/2018 FDA alerts health care professionals and patients not to use sterile drug products from Pharm D Solutions
• 11/8/2018 FDA alerts consumers of Kadesh Incorporation’s voluntary nationwide recall of Puriton Eye Relief Drops due to non-sterile production conditions
• 11/2/2018 FDA alerts patients and health care professionals that some EpiPen auto-injectors may not readily slide out of carrier tube
• 10/11/2018 FDA alerts consumers of Sprayology’s voluntary nationwide recall of homeopathic water-based medicines due to microbial contamination
• 10/4/2018 FDA alerts consumers and pet owners of Silver Star Brand’s voluntary nationwide recall of homeopathic drug products
• 9/14/2018 FDA alerts consumers of BioLyte Laboratories voluntary recall of NeoRelief
• 9/14/2018 FDA alerts consumers not to use products distributed by Years to Your Health
• 9/7/2018 FDA alerts consumers of Beaumont Bio Med’s voluntary recall of all water and alcohol-based products
• 8/31/2018 FDA alerts consumers of HelloLife’s voluntary recall of Neuroveen, Respitrol, Thyroveev and Compulsin
• 8/17/2018 FDA alerts drug makers of a recall of porcine thyroid API from Sichuan Friendly Pharmaceutical Co., Limited, China
• 7/10/2018 FDA announces Ranier’s Rx Laboratory voluntary recall of all sterile compounded drug
• 7/5/2018 FDA advises consumers not to use Blissful Remedies kratom products due to bacterial contamination
• 6/29/2018 FDA advises health care professionals not to use MedGyn Products Monsel’s Solution

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