FDA MedWatch Alerts/Recall Notices (UNOFFICIAL)
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FDA MedWatch Alerts/Recall Notices (UNOFFICIAL)
@fdamedwatch.bsky.social
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Unofficial bot sharing alerts from FDA MedWatch.

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Early Alert: Glucose Monitor Sensor Issue from Abbott Diabetes Care posted 2025-12-02
Additional Details Here.
December 3, 2025 at 11:05 AM
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Recall Alert: Glycar SA Removes Pericardial Patch posted 2025-12-01
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December 2, 2025 at 11:05 AM
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Correction Alert: Becton Dickinson Updates Use Instructions for BD Alaris Pump Issue posted 2025-11-28
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November 29, 2025 at 11:05 AM
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Recall Alert: Baxter Permanently Removes Life2000 Ventilation System posted 2025-11-26
Additional Details Here.
November 27, 2025 at 11:05 AM
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Recall Alert: Max Mobility/Permobil Removes All SpeedControl Dials Used with SmartDrive MX2+ Power Assist Devices posted 2025-11-25
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November 26, 2025 at 11:05 AM
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Early Alert: Large Volume Pump Primary Administration Set Reverse Flow Issue from Fresenius Kabi posted 2025-11-24
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November 25, 2025 at 11:05 AM
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Recall Alert: Intersurgical Inc Removes i-View Video Laryngoscope posted 2025-11-21
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November 22, 2025 at 11:05 AM
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Alert: Medline Industries, LP Removes Certain Sterile Medline Convenience Kits posted 2025-11-20
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November 21, 2025 at 11:05 AM
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Alert: NOxBOX Ltd. Issues Correction for NOxBOXi Nitric Oxide Delivery System Due to Risk for Nitric Oxide Dosing Fluctuations posted 2025-11-20
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November 21, 2025 at 11:05 AM
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Alert: Update to Use Instructions for B Braun Hemodialysis Blood Tubing Set posted 2025-11-19
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November 20, 2025 at 11:05 AM
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Alert: Siemens Healthineers Issues Correction for 3 Tesla MRI Systems posted 2025-11-19
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November 20, 2025 at 11:05 AM
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Update: FDA Encourages the Public to Follow Established Choking Rescue Protocols - FDA Safety Communication posted 2025-11-13
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November 14, 2025 at 11:05 AM
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Fresenius Kabi Issues Voluntary Nationwide Recall of Three Lots of Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL Fill in a 2 mL Vial Due to Out-of-Specification Endotoxin Results in Certain Reserve Samples posted 2025-11-07
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November 8, 2025 at 11:05 AM
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Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 20 mEq Potassium Chloride Injection Due To Overwrap Mislabeled As 10 mEq Potassium Chloride Injection posted 2025-11-03
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November 4, 2025 at 11:05 AM
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Olympus Issues Voluntary Labeling Update for Bronchoscopes Used with Laser Therapy Equipment posted 2025-11-03
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November 4, 2025 at 11:05 AM
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Hintermann Series H3 Total Ankle Replacement Has a Higher-Than-Expected Risk of Device Failure: FDA Safety Communication posted 2025-10-31
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November 1, 2025 at 10:05 AM
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Potential Risks with Certain Uses of Radiofrequency (RF) Microneedling – FDA Safety Communication posted 2025-10-15
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October 16, 2025 at 10:05 AM
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Alert: Automated Impella Controller Correction due to Cybersecurity Issue from Abiomed posted 2025-10-10
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October 11, 2025 at 10:05 AM
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Trividia Health, Inc. Initiates Voluntary Recall of Limited Number of TRUE METRIX® Blood Glucose Meters posted 2025-10-07
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October 8, 2025 at 10:05 AM
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Ventilator Recall: Philips Respironics Removes Certain DreamStation Devices Due to Programming Errors That Can Result in Failed Therapy Modes posted 2025-09-12
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September 30, 2025 at 10:05 AM
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Electrical Wheelchair Component Correction: mo-Vis BVBA Issues Correction for R-net Joysticks Due to a Firmware Error posted 2025-09-16
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September 30, 2025 at 10:05 AM
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Recall and Alert Resources posted 2025-09-29
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September 30, 2025 at 10:05 AM
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Blood and Plasma Warming Device Correction: 3M Company Issues Correction for Ranger Blood/Fluid Warming System posted 2025-09-24
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September 25, 2025 at 10:05 AM
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Endoscopic Aspiration Needle Recall: Olympus Removes Certain ViziShot 2 FLEX (19G) Needles Due to Potentially Deformed A-traumatic Tips posted 2025-09-24
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September 25, 2025 at 10:05 AM
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Early Alert: Automated Impella Controller Purge Retainer Fixation Issue from Abiomed posted 2025-09-23
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September 24, 2025 at 12:20 PM