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Consumer Product Recalls

127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.

October 9, 2025VehiclesNHTSA
Ford 2025 Air Bags recall
Hazard: An air bag that does not deploy as intended increases the risk of injury in a crash.
October 9, 2025VehiclesNHTSA
Braun Ambulances 2023–2026 Vehicle Speed Control recall
Hazard: Failure to turn off the cruise control may cause unexpected acceleration as the brake is released, increasing the risk of crash.
October 9, 2025VehiclesNHTSA
Nissan, Chevrolet 2013–2021 Fuel System, Gasoline recall
Hazard: A blown fuel pump fuse can cause the engine to stall, increasing the risk of a crash.
October 9, 2025VehiclesNHTSA
Heartland, Jayco Fifth Wheel 2026 Equipment recall
Hazard: A murphy bed that falls increases the risk of injury or death.
October 9, 2025VehiclesNHTSA
Dodge 2013–2016 Power Train recall
Hazard: A loss of park function may allow the vehicle to rollaway, increasing the risk of a crash.
October 9, 2025Vehicle EquipmentNHTSA
Mopar Power Train recall
Hazard: A loss of park function may allow the vehicle to rollaway, increasing the risk of a crash.
October 8, 2025Medical DevicesFDA
MedicalCommunications GmbH recalls Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0 (Build 2088) to 2.6.8 (Build 2220). Device Type
Hazard: Potential that the measured value may be smaller than the actual area.
October 8, 2025Medical DevicesFDA
Schiller, Ag recalls Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Hazard: Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
October 8, 2025Medical DevicesFDA
bioMerieux, Inc. recalls VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin formulation cs02n. VITEK¿ 2 is an automated system c
Hazard: Potential for false resistant results for Colistin (cs02n) with multi-drug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii complex used in specific cards
October 8, 2025Medical DevicesFDA
Medline Industries, LP recalls Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q
Hazard: The kits contain certain lots of cannula products where the catheter may not retain its shape.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Vida Fit. Model Number: 11410481.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693,
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio Dot. Model Number: 10684333.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio. Model Number: 10276755.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Numbe
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra fit. Model Number: 10849580.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K1
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Prisma. Model Number: 10849582.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Lumina (DE). Model Number: 11344916.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Connectom.X. Model Number: 11371480.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAGNETOM Cima.X (DE). Model Number: 11647158.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls BIOGRAPH One (DE). Model Number: 11689172.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Biograph mMR. Model Number: 10433372.
Hazard: There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
October 8, 2025Medical DevicesFDA
Howmedica Osteonics Corp. recalls 1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0
Hazard: a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.
October 8, 2025Medical DevicesFDA
Zap Surgical Systems recalls ZAP-X Radiosurgery System, Model: 300150
Hazard: If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error message occurs after the automatic reduction of speed, a software defect could potentially lead the collimator to collide with patient shoulders or the patient table.
October 8, 2025Medical DevicesFDA
Bard Peripheral Vascular Inc recalls Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the Vencl
Hazard: Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is executed immediately upon catheter connection to the generator, occurring before the procedure interface becomes accessible. When a catheter fails this verification process, the generator displays a Red X indicator on the screen without accompanying error codes, effectively disabling catheter functionality. However, BD has determined that software version 3.35 generates false positive failures due to temperature-dependent verification parameters, incorrectly flagging properly functioning Venclose EVSRF Ablation Catheters as defective when the catheter temperature is not at steady state during the check initiation.
October 8, 2025Medical DevicesFDA
North American Rescue LLC. recalls JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete (Mod
Hazard: Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.
October 8, 2025Medical DevicesFDA
Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Product
Hazard: The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.