Class IIOngoingZ-1229-2026
VANTIVE US HEALTHCARE LLC recalls PRISMAFLEX HF1000 SET
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
VANTIVE US HEALTHCARE…ILFeb 11, 2026
Class II recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,225–1,236 of 3,866 recalls
Class IIOngoingZ-1228-2026
VANTIVE US HEALTHCARE LLC recalls PRISMAFLEX M150 SET
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
VANTIVE US HEALTHCARE…ILFeb 11, 2026
Class IIOngoingZ-1227-2026
VANTIVE US HEALTHCARE LLC recalls PRIMSAFLEX M100 SET
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
VANTIVE US HEALTHCARE…ILFeb 11, 2026
Class IIOngoingZ-1226-2026
VANTIVE US HEALTHCARE LLC recalls OXIRIS SET
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
VANTIVE US HEALTHCARE…ILFeb 11, 2026
Class IIOngoingZ-1225-2026
VANTIVE US HEALTHCARE LLC recalls PRISMAFLEX ST150 SET US
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
VANTIVE US HEALTHCARE…ILFeb 11, 2026
Class IIOngoingZ-1224-2026
VANTIVE US HEALTHCARE LLC recalls PRISMAFLEX ST100 SET US
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
VANTIVE US HEALTHCARE…ILFeb 11, 2026
Class IIOngoingZ-1223-2026
Olympus Corporation Of The Americas recalls Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus Single Use E…
A deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.
Olympus Corporation of…PAFeb 11, 2026
Class IIOngoingZ-1222-2026
Olympus Corporation Of The Americas recalls Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single Use Electros…
A deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.
Olympus Corporation of…PAFeb 11, 2026
Class IIOngoingZ-1221-2026
Beckman Coulter, Inc. recalls COULTER DxH Diluent
Due to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers.
Beckman Coulter, Inc.FLFeb 11, 2026
Class IIOngoingZ-1220-2026
Miach Orthopaedics recalls BEAR Implant. Model Number: 1000.
Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will also be incorrect.
Miach OrthopaedicsMAFeb 4, 2026
Class IIOngoingZ-1219-2026
LSL Healthcare Inc. recalls LSL Healthcare
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
LSL Healthcare Inc.ILFeb 4, 2026
Class IIOngoingZ-1218-2026
LimFlow, Inc. recalls Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Incorrect expiration date
LimFlow, Inc.CAFeb 4, 2026