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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
February 12, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013
Hazard: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
February 12, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
Hazard: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
February 12, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C System Code: (1) 722001
Hazard: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
February 12, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027
Hazard: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
February 12, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026
Hazard: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
February 12, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura CV20 System Code: 722031
Hazard: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
February 12, 2025Medical DevicesFDA
Oxoid Limited recalls Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797
Hazard: Mislabeling; Levofloxacin Antimicrobial susceptibility disc packaging may contain Norfloxacin Antimicrobial Susceptibility discs.
February 12, 2025Medical DevicesFDA
LivaNova USA, Inc. recalls SenTiva, REF: 1000C, Generators Part of the VNS Therapy System with Microburst Stimulation. Used for Vagus Nerve Stimul
Hazard: Vagus nerve stimulator generators may stop delivering stimulation due to an internal, mechanically activated component that may become stuck in a closed position, which may result in patients returning to baseline seizure frequency or depressive symptoms and in the longer term, patients may be required to undergo generator replacement surgery to replace their device.
February 12, 2025Medical DevicesFDA
LivaNova USA, Inc. recalls SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve Stimula
Hazard: Vagus nerve stimulator generators may stop delivering stimulation due to an internal, mechanically activated component that may become stuck in a closed position, which may result in patients returning to baseline seizure frequency or depressive symptoms and in the longer term, patients may be required to undergo generator replacement surgery to replace their device.
February 12, 2025Medical DevicesFDA
ROi CPS LLC recalls regard Item Number: 830106006, LD01114F - Newborn Kit containing the component Neo-Tee Resuscitator. Convenience kit to
Hazard: There is a potential for the Inline Controller to be using the spring out of specification causing a loss of positive pressure resulting in the Neo-Tee Resuscitator and/or Circuit will not reach the high and low ends of the PIP and PEEP pressure ranges impacting effective ventilation of the patient..
February 12, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Optima XR646 HD. X-Ray imaging system.
Hazard: The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.
February 12, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Discovery XR656 HD. X-Ray imaging system.
Hazard: The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.
February 12, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Discovery XR656HD. X-Ray imaging system.
Hazard: The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.
February 12, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709). X-Ray imaging system.
Hazard: The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.
February 12, 2025Medical DevicesFDA
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Indicated for use in a hospital and in outpatient care enviro
Hazard: Large Volume Pump Software, version 5.9.2 and earlier has potential for the following anomalies: 1. The pump may become nonfunctional if during an alarm condition the Pause Audio option is repeated 70 time or more. 2. If a secondary infusion is started at the exact moment a primary infusion completes and VTBI reaches 0, it will switch to primary. The primary infusion will infuse at the previously programed primary rate and continue until the infusion is stopped or the bag is empty.
February 12, 2025Food & BeverageFDA
Mutual Trading Company Inc. recalls Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite side
Hazard: Imported Monkfish Liver undeclared allergen (Milk)
February 12, 2025Food & BeverageFDA
La Fiesta Food Products recalls La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned, NET WT 8 OZ. (227g), UPC# 032327000887
Hazard: Firm distributed a Seasoned Bread Crumb product with undeclared allergen (Sesame) not on the label.
February 12, 2025Food & BeverageFDA
La Fiesta Food Products recalls La Fiesta PAN RAYADO Bread Crumbs, NET WT 8 OZ. (227g), UPC# 032327000886
Hazard: Firm distributed a Bread Crumb product with undeclared allergen (Sesame) not on the label.
February 12, 2025Food & BeverageFDA
D. Coluccio & Sons Inc. recalls COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES
Hazard: Contains undeclared visible almonds
February 12, 2025Food & BeverageFDA
COREPACK MANUFACTURING INC recalls White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.
Hazard: Possible Salmonella contamination of affected product.
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8202891 PLAIN VANILLA MINI CAKE DONUT RING BULK 240X1.25OZ, NET WT 16.88 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8202731 UNFLD BISMARK DONUT PFD 78X3OZ, NET WT 13.16 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201936 NATURAL & ARTIFICIAL FLAVORED BAVARIAN BISMARK, NET WT 13.16 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201927 APPLE FRITTER DONUT PFD 70 X 3.5OZ, NET WT 13.78 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201926 FBALL/EGG SHPD DONUT PFD 78 X 2OZ, NET WT 8.78 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201923 BAV CRM BAR DONUT PFD 78 X 3OZ, NET WT 13.16 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201922 FLAVORED RASPBERRY BISMARK PFD 3OZ, NET WT 13.16 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201921 FRENCH CRULLER PFD 72x1.6 OZ, NET WT 6.48 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201920 APPLE CRISP CK DONUT PFD 78x3OZ, NET WT 13.16 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201919 BAR YST DONUT UNFLD PFD 74x3OZ, NET WT 12.49 LB
Hazard: potential for contamination with listeria monocytogenes