US FDA MedWatch @FDAMedWatch
Clinically important safety information on human medical products from FDA. Comments: [email protected] Privacy: https://t.co/xpVlP2hVsL fda.gov/medwatch Silver Spring, MD Joined October 2010-
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BioMérieux Inc. Recalls VITEK 2 AST Kit due to Incorrect Ceftriaxone Concentrations fda.gov/medical-device…
SonarMed Inc. Recalls Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty fda.gov/medical-device…
SonarMed Inc. Recalls Airway Monitors Due to a Software Anomaly Resulting in Failure to Detect a Partial Obstruction in 2.5mm Sensors and Up To 3mm Distal to the Sensor Tip fda.gov/medical-device…
Elekta Instrument AB Recalls Disposable Biopsy Needle Kit for Leksell Stereotactic System for Possibly Containing Microscopic Stainless-Steel Debris on the Inside of the Biopsy Needle fda.gov/medical-device…
InfuTronix, LLC Recalls Nimbus and Nimbus II Infusion Pump Systems for Multiple Device Failures That May Cause Severe Injury and Death fda.gov/medical-device…
Draeger, Inc. Recalls Perseus A500 Anesthesia System for Risk of Sudden Unexpected Shutdown When Used on Battery Power fda.gov/medical-device…
Outset Medical, Inc. Recalls Tablo Hemodialysis System for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA fda.gov/medical-device…
Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and Stay-Safe /Luer Lock Adapter for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA fda.gov/medical-device…
DeRoyal Industries, Inc. Recalls Tracecarts Containing 16FR Urine Meter Foley Under Recall by Nurse Assist fda.gov/medical-device…
Sapropterin Dihydrochloride Powder for Oral Solution 100 mg by Dr. Reddy's: Recall - Due to Sub-Potency fda.gov/safety/recalls…
Schwinnng Capsules by STOP CLOPEZ CORP: Recall - Due to the Presence of Undeclared Nortadalafil fda.gov/safety/recalls…
FDA Encourages the Public to Follow Established Choking Rescue Protocols - FDA Safety Communication fda.gov/medical-device…
Fresenius Kabi USA, LLC Recalls Ivenix Infusion Pump LVP Software for Anomalies That Have the Potential to Cause Serious Patient Harm or Death fda.gov/medical-device…
Boston Scientific Recalls Obsidio Embolic for Bowel Ischemia Risk fda.gov/medical-device…
Abbott/Thoratec Corp. Recalls Heartmate II and Heartmate 3 Left Ventricular Assist System (LVAS) Due to Long-term Buildup of biological material Causing an Obstruction fda.gov/medical-device…
Tejocote Products by Global Mix: Recall - Because of Possible Health Risk fda.gov/safety/recalls…
Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel by Aruba Aloe Balm N.V.: Recall: Due to Presence of Methanol fda.gov/safety/recalls…
Honeywell Fendall 2000 Non-Sterile Eyewash Cartridges # 32-002050-0000 Used with the Fendall 2000 Eyewash Station by Honeywell Safety Products USA: Recall - Due to a Lack of Appropriate Policies and Procedures by Honeywell’s Supplier fda.gov/safety/recalls…
ForeverMen by FAonline: Recall - Due Presence of Sildenafil and Tadalafil fda.gov/safety/recalls…
Smiths Medical ASD Recalls PneuPac ParaPAC Plus 300 and 310 Ventilator Kits for a Malfunction Causing Non-Cycling, Continuous Positive Gas Flow and Preventing Proper Ventilation fda.gov/medical-device…
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Deb Autor, Chair of the FDA Alumni Association presents the group’s annual Wiley Award for a lifetime of dedicated public health service to FDA Principal Deputy Commissioner Dr. Janet Woodcock.
Thank you to all the nurses in the United States and around the world for all that you do to keep us safe every day and especially now during the #COVID19 pandemic. We are safer and healthier as a nation because of what you do. #NationalNursesWeek
Thank you to all the nurses in the United States and around the world for all that you do to keep us safe every day and especially now during the #COVID19 pandemic. We are safer and healthier as a nation because of what you do. #NationalNursesWeek
To all of the nurses across the country, THANK YOU for all that you do each and every day. Now more than ever, we are especially grateful for your efforts to keep us safe during the #COVID19 pandemic. #ThankYouNurses
I want to take a moment to recognize the FDA workforce as well as fellow public servants during Public Service Recognition Week. Now more than ever, they deserve strong recognition & support for their efforts during these unprecedented and challenging times. #PSRW #HHS_IttakesYOU
To nurses across the United States going above and beyond to keep us safe, thank you. #NationalNursesDay #NW2020
In the event that an adverse drug event is suspected or observed from any medication used to prevent/treat #COVID19, we encourage health care providers to submit a report to @FDAMedWatch. COVID-19 or #coronavirus should be referenced in submitted reports. spr.ly/601112DFz
Thanks @TuckerCarlson for having me on the show tonight to talk about how the @US_FDA team is hard at work combating #COVID19 by supporting drug treatment and vaccine development.
For those who have been tracking, #FDA has completed review of all available data on the use of Nuplazid - no new or unexpected safety findings have been identified; health care providers reminded to follow prescribing information go.usa.gov/xPT98
Next up to speak is Patient Affairs Staff (PAS) Acting Director Andrea Furia-Helms. #CDERandUEngagementWorkshop
Gericare Eye Wash by Kareway Products: Recall - Potential Product Contamination go.usa.gov/xnATC
Codeine and tramadol can cause breathing problems for children. Beware of giving kids these medicines. go.usa.gov/x5g9a
Clinicians: take a minute to learn about reporting problems to FDA - view the MedWatch Minute video today! youtu.be/s6LrPeXG7Fo
Webinar today 1 pm! MedWatch: Voluntarily Reporting Problems to FDA. Featuring Cristina Klafehn, PharmD, BCPS, CDE go.usa.gov/xWdMG
Opioid Pain/Cough Medicines Combined w/ Benzodiazepines: FDA Requiring Boxed Warning About Serious Risks and Death go.usa.gov/xWRqj
FDA Webinar - Intro to Post-Marketing Drug Safety Surveillance: Pharmacovigilance in FDA/CDER 02/23/2016, go.usa.gov/cpxn9