Class IIOngoingZ-0121-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Set
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Recalls: Process control
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 481–492 of 822 recalls
Class IIOngoingZ-0120-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0119-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0118-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0117-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm)…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0116-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm)…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0115-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm)…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0114-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tu…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0072-2026
LeMaitre Vascular, Inc. recalls Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.
LeMaitre Vascular, Inc…NJOct 15, 2025
Class IIOngoingZ-0038-2026
ImaCor Inc. recalls ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound miniaturized TE…
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
ImaCor Inc.NYOct 15, 2025
Class IOngoingZ-2617-2025
Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software…
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Draeger, Inc.PAOct 8, 2025
Class IOngoingZ-2616-2025
Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Ve…
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
Draeger, Inc.PAOct 8, 2025