Class IIOngoingZ-2170-2025
Stryker Corporation recalls Stryker
Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.
Stryker CorporationCAJul 30, 2025
Recalls in California
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 253–264 of 439 recalls
Class IIOngoingZ-2152-2025
Beckman Coulter Inc. recalls Estrone RIA
A specific lot of bovine serum albumin (BSA) used for manufacturing of coated tubes (CT) that are included in the Estrone RIA kit lots caused different affinity of manufactured coated tubes to patient samples, causing fa…
Beckman Coulter Inc.CAJul 30, 2025
Class IIOngoingZ-2116-2025
ICU Medical, Inc. recalls SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve
Due to a manufacturing issue, disinfecting cap for needle-free connectors may have an incomplete seal between the foil lid and plastic container, which may result in isopropyl alcohol evaporation from the sponge, which m…
ICU Medical, Inc.CAJul 23, 2025
Class IIOngoingZ-2107-2025
Preat Corp recalls Preat
Due to manufacturing error, digital analog rotational feature is 180 degrees off.
Preat CorpCAJul 16, 2025
Class IIOngoingZ-2100-2025
Neurovision Medical Products Inc recalls Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Ca…
Product packaging contains the wrong part number and kit contents.
Neurovision Medical Pr…CAJul 16, 2025
Class IIOngoingZ-2099-2025
Canary Medical, Inc. recalls Brand Name: Canturio¿ Smart Extension Product Name: CSE Implant Model/Catalog Number:…
Due to labeling error. Product incorrectly labeled.
Canary Medical, Inc.CAJul 16, 2025
Class IOngoingZ-2085-2025
Edwards Lifesciences, LLC recalls Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: F…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Edwards Lifesciences,…CAJul 16, 2025
Class IOngoingZ-2084-2025
Edwards Lifesciences, LLC recalls Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number:…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Edwards Lifesciences,…CAJul 16, 2025
Class IOngoingZ-2083-2025
Edwards Lifesciences, LLC recalls Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number:…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Edwards Lifesciences,…CAJul 16, 2025
Class IOngoingZ-2082-2025
Edwards Lifesciences, LLC recalls Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number:…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Edwards Lifesciences,…CAJul 16, 2025
Class IOngoingZ-2081-2025
Edwards Lifesciences, LLC recalls Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/C…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Edwards Lifesciences,…CAJul 16, 2025
Class IOngoingZ-2080-2025
Edwards Lifesciences, LLC recalls Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/C…
due to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.
Edwards Lifesciences,…CAJul 16, 2025