Class IIOngoingZ-2299-2026
CareFusion 303, Inc. recalls BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303, Inc.CAJun 10, 2026
Recalls in California
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 25–36 of 439 recalls
Class IIOngoingZ-2298-2026
CareFusion 303, Inc. recalls BD Pyxis MedStation ES REF: 323 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303, Inc.CAJun 10, 2026
Class IIOngoingZ-2297-2026
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
CareFusion 303, Inc.CAJun 10, 2026
Class IIOngoingZ-2294-2026
Shimadzu Medical Systems recalls Digital Angiography System Trinias:UD150G-40 / D150GC-40
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
Shimadzu Medical Syste…CAJun 10, 2026
Class IIOngoingZ-2283-2026
Advanced Bionics, LLC recalls Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mi…
Due to incorrect shelf-life expiration date.
Advanced Bionics, LLCCAJun 10, 2026
Class IIOngoingZ-2210-2026
ICU Medical, Inc. recalls Oncology Kit w/60" (152 cm) Appx 2.2 ml
Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption…
ICU Medical, Inc.CAMay 27, 2026
Class IIOngoingZ-2204-2026
Becton, Dickinson And Company recalls Swan-Ganz Pacing Catheter
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Becton, Dickinson and…CAMay 27, 2026
Class IIOngoingZ-2203-2026
Becton, Dickinson And Company recalls Swan-Ganz Jr Catheter
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Becton, Dickinson and…CAMay 27, 2026
Class IIOngoingZ-2202-2026
Becton, Dickinson And Company recalls Swan-Ganz Catheter
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Becton, Dickinson and…CAMay 27, 2026
Class IIOngoingZ-2200-2026
MICROVENTION INC. recalls LVIS Intraluminal Support Device
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration.…
MICROVENTION INC.CAMay 20, 2026
Class IIOngoingZ-2172-2026
Edwards Lifesciences, LLC recalls Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.
Edwards Lifesciences,…CAMay 20, 2026
Class IIOngoingZ-2169-2026
Quidel Corporation recalls QuickVue Dipstick Strep A Test
Product has the potential for false positive results
Quidel CorporationCAMay 20, 2026