Recalls affecting Iowa
Notices that name Iowa in their distribution area, plus every nationwide recall — nationwide recalls reach Iowa too.
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Class I · 11 days ago
A&p Creations X10 Natural Enhancement Supplement, 0.5 fl oz/sachet , 7 sachets/box recall: Product contains undeclared Sildenafil and Tadalafil
Product contains undeclared Sildenafil and Tadalafil.
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NHTSA safety recall · 16 days ago
Volvo Car EX30 and EX30CC recall: The head restraint cushion may detach during a crash
The head restraint cushion may detach during a crash.
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NHTSA safety recall · 17 days ago
Honda recall: When using the tire repair kit, pressure may build within the sealant bottle
When using the tire repair kit, pressure may build within the sealant bottle, causing the bottle cap to detach.
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Highest risk · 17 days ago
Giant Bicycle LED-Light Keys Included with SureLock Bike Lock Sets recall: Risk of Serious Injury or Death from Battery Ingestion
Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
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Highest risk · 17 days ago
DR Power Equipment Pilot and Premier Trimmer Mowers recall: Risk of Serious Injury or Death from Fire and Burn Hazards
Risk of Serious Injury or Death from Fire and Burn Hazards
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Highest risk · 17 days ago
Decathlon America Van Rysel GRVL AF Bicycles recall: Risk of Serious Injury or Death from Crash Hazard
Risk of Serious Injury or Death from Crash Hazard
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NHTSA safety recall · 18 days ago
Toyota RAV4 Plug-In Hybrid recall: The motor generator ECU may encounter an error
The motor generator ECU may encounter an error, causing the plug-in-hybrid system to reduce power or shutdown when driven at higher speeds.
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Class II · 18 days ago
Philips North America SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T recall: When exporting diffusion tensor imaging (DTI) scans from a MR system using
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data…
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Class II · 18 days ago
Hopkins Telescope 30¿, 4mm REF 10005BA Udi-Di code: 04048551045121 Karl recall: Due to incorrect inside packaging label for eyepiece
Due to incorrect inside packaging label for eyepiece.
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Class II · 18 days ago
Brand Name: ASP Global Product Name:Disposable Tourniquet Cuff recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
ASP Global, LLC. Brand Name: MPR Product Name:Single USE Tourniquet Cuff 15" 1 Line recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
ASP Global, LLC. Brand Name: Expressaire Product Name: Disposable Tourniquet Cuff recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
NOxBOXi Nitric Oxide Delivery System recall: Potential for irregular oxygen readings due to a manufacturing issue
Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.
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Class II · 18 days ago
Heraeus Medical GmbH Palacos R pro 40 recall: Potential for monomer liquid leakage
Potential for monomer liquid leakage.
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Class II · 18 days ago
Percussionaire Corporation Intrapulmonary Percussive Ventilation, IPV 1 recall: Labeling updated warning not to use Intrapulmonary percussive ventilation
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV…
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Class II · 18 days ago
Brand Name: ASP Global Product Name:Disposable Tourniquet Cuff recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
ASP Global, LLC. Brand Name: Expressaire Product Name:Disposable Tourniquet Cuff recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
Alere San Diego, Inc. Fisher Scientific Sure-Vue Urine hCG Strip recall: hCG rapid tests may detect low levels of hCG below the stated assay
hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.
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Class II · 18 days ago
ASP Global, LLC. Brand Name: MPR Product Name:Single USE Tourniquet Cuff 24" 2 Line recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
ASP Global, LLC. Brand Name: Expressaire Product Name:Disposable Tourniquet Cuff recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
ASP Global, LLC. Brand Name: Expressaire Product Name:Disposable Tourniquet Cuff recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography recall: Positron emission tomography and computed tomography x-ray systems have
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS…
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Class II · 18 days ago
ASP Global, LLC. Brand Name: MPR Product Name:Single USE Tourniquet Cuff 34" 2 Line recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…
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Class II · 18 days ago
ASP Global, LLC. Brand Name: Expressaire Product Name: Disposable Tourniquet Cuff recall: Due to incorrect expiration date on product manufactured between September
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The…