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US FDA MedWatch

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Clinically important safety information on human medical products from FDA. Comments: [email protected] Privacy: https://t.co/xpVlP2hVsL

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Silver Spring, MD
Joined October 2010
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@FDAMedWatch
US FDA MedWatch
@FDAMedWatch
6 days
ReBoost Nasal Spray by MediNatura New Mexico: Recall - Due to Microbial Contamination https://t.co/VSKACBLVl5
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US FDA MedWatch
@FDAMedWatch
7 days
Early Alert: Anesthesia System Issue from GE HealthCare https://t.co/zVmmemHs1x
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US FDA MedWatch
@FDAMedWatch
14 days
Correction Alert: Olympus Updates Use Instructions for Ligating Device https://t.co/4OKUp2LPX7
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US FDA MedWatch
@FDAMedWatch
15 days
Early Alert: Glucose Monitor Sensor Issue from Abbott Diabetes Care https://t.co/mwgYnZsQ4I
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US FDA MedWatch
@FDAMedWatch
19 days
Correction Alert: Becton Dickinson Updates Use Instructions for BD Alaris Pump Issue https://t.co/MmR9x0mLlm
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@FDAMedWatch
US FDA MedWatch
@FDAMedWatch
21 days
Recall Alert: Baxter Permanently Removes Life2000 Ventilation System https://t.co/6nTiwV7VBM
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US FDA MedWatch
@FDAMedWatch
21 days
Recall Alert: BALT USA Removes MEGA Ballast Distal Access Platform https://t.co/JSu7BpZA7Z
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@FDAMedWatch
US FDA MedWatch
@FDAMedWatch
22 days
Recall Alert: Max Mobility/Permobil Removes All SpeedControl Dials Used with SmartDrive MX2+ Power Assist Devices https://t.co/Os2mxQIvVf
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US FDA MedWatch
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23 days
Early Alert: Large Volume Pump Primary Administration Set Reverse Flow Issue from Fresenius Kabi https://t.co/CgwywkNQQ6
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US FDA MedWatch
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26 days
Recall Alert: Intersurgical Inc Removes i-View Video Laryngoscope https://t.co/IuLyIrfAoZ
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US FDA MedWatch
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26 days
Correction Alert: Medline Industries, LP Updates Use Instructions for Medline Kits Containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles https://t.co/F2b9eBHHz6
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US FDA MedWatch
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26 days
Alert: NOxBOX Ltd. Issues Correction for NOxBOXi Nitric Oxide Delivery System Due to Risk for Nitric Oxide Dosing Fluctuations https://t.co/G5YUiPTWY7
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@FDAMedWatch
US FDA MedWatch
@FDAMedWatch
26 days
Alert: NOxBOX Ltd. Issues Correction for NOxBOXi Nitric Oxide Delivery System Due to Rapid Command Input Issue https://t.co/eajQb5cUuX
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US FDA MedWatch
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28 days
Alert: Siemens Healthineers Issues Correction for 3 Tesla MRI Systems https://t.co/0uWOrfOkp3
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US FDA MedWatch
@FDAMedWatch
28 days
Alert: Updated Use Instructions for B Braun Medical Hemodialysis Blood Tubing Set https://t.co/GnGPqBDRi2
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@FDAMedWatch
US FDA MedWatch
@FDAMedWatch
1 month
Whole Nutrition Infant formula 24 oz cans and 0.6 oz packets by ByHeart: Recall - Due to Potential Foodborne Illness – Clostridium botulinum https://t.co/1atEOIJmyK
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US FDA MedWatch
@FDAMedWatch
1 month
Three Lots of Famotidine Injection USP, 20 mg per 2 mL (10 mg per mL), 2 mL Fill in a 2 mL Vial by Fresenius Kabi: Recall - Due to Out-of-Specification Endotoxin Results in Certain Reserve Samples https://t.co/4YHL9pHp6c
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US FDA MedWatch
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1 month
20 mEq Potassium Chloride Injection by Otsuka ICU Medical: Recall - Due To Overwrap Mislabeled As 10 mEq Potassium Chloride Injection https://t.co/8v8v5Dls7U
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US FDA MedWatch
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2 months
Update on Hintermann Series H3 Total Ankle Replacement Post-Approval Study Data: FDA Safety Communication https://t.co/rBiBVLoZrL
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@FDAMedWatch
US FDA MedWatch
@FDAMedWatch
2 months
Potential Risks with Certain Uses of Radiofrequency (RF) Microneedling: Safety Communication https://t.co/lZKFgNMHe5
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