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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 23, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn Spot Vital Signs 4400 Device, Product Code/Part Numbers: 1) 44WT-2; 2) 44WT-3; 3) 44WT-4; 4) 44WT-6
Hazard: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
April 23, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A; 2) ) Pr
Hazard: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
April 23, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B; 2) 74CE-B; 3) 74CT-B; 4) 74
Hazard: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
April 23, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn Connex Integrated Wall System, Product Code/Part Numbers: 1) 84MTVE2-4; 2) 84MTVE2-6; 3) 84MTVE2-B;
Hazard: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
April 23, 2025Medical DevicesFDA
Straumann USA LLC recalls TLX/TLC SP Guided Implant Driver, for ratchet, stainless steel; REF: 037.3002;
Hazard: The devices are missing the laser marked depth markings.
April 23, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn CP150 Electrocardiograph:
Hazard: There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
April 23, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn CONNEX Accessory Power Management Stand:
Hazard: There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
April 23, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor (CVSM):
Hazard: There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.
April 23, 2025Medical DevicesFDA
Abbott Medical recalls Aveir DR Leadless Pacemaker (LP) Ventricular Device REF LSP202V UDI-DI code: 05415067040725 REF LSP112V UDI-DI cod
Hazard: Due to a manufacturing issue, leadless pacemakers may have been exposed to higher than normal temperatures which may result in premature battery failure.
April 23, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Venue Fit Models: R3 (Model Number H45303VFSC, H45303VFSW), R4 (Model Number H45314VFS, H45314VFSW), Venue Fit R5 system
Hazard: The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
April 23, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H
Hazard: The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
April 23, 2025Medical DevicesFDA
Philips North America Llc recalls Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Hazard: Potential for collimator to fall as a result of incorrect installation.
April 23, 2025Medical DevicesFDA
Philips North America Llc recalls Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
Hazard: Potential for collimator to fall as a result of incorrect installation.
April 23, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK
Hazard: If "Clear All" selected medications is selected on patient profile, the automated dispensing cabinet may allow dispensing of medication without first requiring the RxVerify Validation Code be entered/without validation from a pharmacist, which could lead to unintended and incorrect medication removal.
April 23, 2025Medical DevicesFDA
ZOLL Circulation, Inc. recalls Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200 (C
Hazard: AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 22714183-5 Software Version: N/A Pr
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 227-5 Software Version: N/A Product
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 2271418-5 Software Version: N/A Pro
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 2210-5 Software Version: N/A Produc
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 220135 Software Version: N/A Produc
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 20083 Software Version: N/A Product
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 210 Software Version: N/A Product D
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 198 Software Version: N/A Product D
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Tandem Diabetes Care, Inc. recalls Tandem Mobi Insulin Pump with Interoperable Technology
Hazard: A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.
April 23, 2025Medical DevicesFDA
Tandem Diabetes Care, Inc. recalls t:slim X2 Insulin Pump with Interoperable Technology
Hazard: A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.
April 23, 2025Medical DevicesFDA
Bard Access Systems, Inc. recalls BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196, 9174118
Hazard: Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.
April 23, 2025Food & BeverageFDA
Grain Millers Inc recalls Rolled Oats packaged in Bulk Poly Supersacks packaged and labeled as follows: 1. 1800 LB Regular Rolled Oats #5, Weig
Hazard: Potential Foreign material (plastic)
April 23, 2025Food & BeverageFDA
Blooming Import Inc. recalls Golden Crop Candy (8 oz. (227g) un-wrapped candies)
Hazard: Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
April 23, 2025Food & BeverageFDA
Blooming Import Inc. recalls Golden Crop Candy (10 oz. (283g) wrapped candies)
Hazard: Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
April 23, 2025Food & BeverageFDA
La Mexicana Tortilla Factory, Inc. recalls Tortilla Chip Green 4 cut packed 5lbs per bag; 6 bags per box
Hazard: Undeclared Yellow #5