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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
October 16, 2025Sports & RecreationCPSC
Textron E-Z-GO Recalls Personal Transportation Vehicles Due to Risk of Serious Injury and Fire Hazard
Hazard: The recalled PTV can leak fuel at the quick-connect fitting between the fuel line and the fuel injector mounted on the engine, posing a risk of serious injury and fire hazard.
October 16, 2025VehiclesNHTSA
Alexis Fire Equipment 2020–2025 Latches/Locks/Linkages recall
Hazard: A door that cannot be opened may trap occupants inside the vehicle, increasing the risk of injury.
October 16, 2025VehiclesNHTSA
Land Rover, Jaguar 2025–2026 Power Train recall
Hazard: A gear shift position indicator that fails to illuminate can make it difficult to identify the correct transmission gear position, increasing the risk of a crash.
October 16, 2025VehiclesNHTSA
Cadillac, Chevrolet 2025–2026 Tires recall
Hazard: Tire tread detachment increases the risk of a crash.
October 15, 2025Medical DevicesFDA
Applied Medical Technology Inc recalls NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NRT-06090-I The NutraGlide Nasal Feeding Tub
Hazard: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
October 15, 2025Medical DevicesFDA
Applied Medical Technology Inc recalls NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-I The NutraGlide Nasal Feeding Tub
Hazard: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
October 15, 2025Medical DevicesFDA
Applied Medical Technology Inc recalls NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding Tub
Hazard: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
October 15, 2025Medical DevicesFDA
Applied Medical Technology Inc recalls NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding Tub
Hazard: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls Design Options, PERIFIX FX Epidural Anesthesia Tray. Product Code: CESK. Product Descriptions: 1. CESK ROBERT WOOD J
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls Combined Spinal and Epidural Anesthesia Tray 2, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga.
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls Design Options, Pain Management Tray. Product Code: SESK. Product Descriptions: 1. SESK PARKLAND MEMORIAL FX CSE TRAY.
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle - 17 Ga. x 3-1/2 in. (8.9 cm) - Winged, PER
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 1
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 1
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray, 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Fixed Wings, 19 Ga.
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged a
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged a
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm) Tuohy Epidural Needle - Winged an
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and
Hazard: Potential for the lid of the catheter connector to be in the incorrect position.
October 15, 2025Medical DevicesFDA
Inpeco S.A. recalls FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic
Hazard: The FlexLab X System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples. This function has not been evaluated for safety and effectiveness by the FDA, so its use may cause an increase in erroneous results or a delay in patient results.
October 15, 2025Medical DevicesFDA
Inpeco S.A. recalls FlexLab (FLX) System. Potassium Test System. in vitro diagnostic
Hazard: The FlexLab System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples. This function has not been evaluated for safety and effectiveness by the FDA, so its use may cause an increase in erroneous results or a delay in patient results.
October 15, 2025Medical DevicesFDA
LeMaitre Vascular, Inc. recalls Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegr
Hazard: Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.
October 15, 2025Medical DevicesFDA
Beckman Coulter Inc. recalls SYNCHRON Systems Phosphorus (PHOSm) Reagent REF: 467868 For In Vitro Diagnostic Use, Rx Only.
Hazard: Specific SYNCHRON Systems Modular Chemistry Phosphorus (PHOSm REF 467868) reagent lots may fail calibration before the lot expiration date which causes a delay in obtaining patient results.
October 15, 2025Medical DevicesFDA
Abiomed, Inc. recalls Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding
Hazard: Potential cybersecurity vulnerabilities related to the operating system in the Automated Impella Controller (AIC).
October 15, 2025Medical DevicesFDA
GE Medical Systems, SCS recalls AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2
Hazard: Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.
October 15, 2025Medical DevicesFDA
FUJIFILM Healthcare Americas Corporation recalls FDR Visionary Suite, CH-200 Model/Version Numbers: (1) 566-16130-23, (2) 566-16130-31, (3) 566-16130-33
Hazard: It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was broken while being operated toward the front while lifting.
October 15, 2025Medical DevicesFDA
Fresenius Medical Care Holdings, Inc. recalls Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX F160NRe 12/CS 1.5SA EBEAM, (2) 0500318E OPTIFL
Hazard: To provide further information to the user to ensure proper use of the medical device. the caps had been changed from a threaded version to a press-on version whereby the user must press the caps firmly onto the dialyzer to securely affix the cap.
October 15, 2025Medical DevicesFDA
CORNEAT VISION, LTD. recalls EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, S
Hazard: Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.