Recalls affecting Delaware
Notices that name Delaware in their distribution area, plus every nationwide recall — nationwide recalls reach Delaware too.
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Highest risk · 1+ years ago
Polaris Industries Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP recall: Risk of Serious Injury from Fire Hazard
Risk of Serious Injury from Fire Hazard
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Highest risk · 1+ years ago
Knog Bicycle Lights recall: Fire and Burn Hazards
Fire and Burn Hazards
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Highest risk · 1+ years ago
Grundens Youth Jackets with Drawstrings recall: Strangulation Hazard; Risk of Serious Injury or Death
Strangulation Hazard; Risk of Serious Injury or Death
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Class I · 1+ years ago
Hoque Dry Ghoinnya Fish recall: Product was found to be uneviscerated. Uneviscerated fish have been linked
Product was found to be uneviscerated. Uneviscerated fish have been linked to outbreaks of botulism poisoning.
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NHTSA safety recall · 1+ years ago
Mazda North American Operations CX-50 and CX-50 Hybrid recall: The front suspension fastener bolts may not be tightened properly
The front suspension fastener bolts may not be tightened properly, which can result in suspension component and/or wheel detachment.
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 266122 recall: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for…
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Class II · 1+ years ago
HeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03 recall: Due to customer complaints, defibrillator pads may contain damage pins
Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.
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Class II · 1+ years ago
Becton Dickinson & Co. BD Phoenix M50 Instrument recall: Product service credentials used by some BD technical support teams to access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Class II · 1+ years ago
Becton Dickinson & Co. BD MAX System, for in vitro diagnostic use recall: Product service credentials used by some BD technical support teams to access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Class II · 1+ years ago
Synthes Products LLC LOW Prof Lckng Screw, F/IM Nail 5.0MM / L recall: Although the etched length on the screw is correct
Although the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged…
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Class II · 1+ years ago
Beckman Coulter, Inc. DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE recall: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access
Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct…
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Class II · 1+ years ago
Becton Dickinson & Co. BD Bactec Blood Culture System recall: Product service credentials used by some BD technical support teams to access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E recall: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for…
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Class II · 1+ years ago
Becton Dickinson & Co. BD Veritor Connect Software recall: Product service credentials used by some BD technical support teams to access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Class I · 1+ years ago
B Braun Medical Inc Brand Name: Hemodialysis Bloodlines Product Name: Streamline recall: The potential for micro-air bubbles observed in the bloodline and air-in-line
The potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 266197 recall: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for…
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Class II · 1+ years ago
Becton Dickinson & Co. BD Bactec Blood Culture System recall: Product service credentials used by some BD technical support teams to access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Class II · 1+ years ago
Beckman Coulter, Inc. DxI 9000 Access Immunoassay Analyzer recall: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access
Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct…
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Class I · 1+ years ago
Abiomed, Inc. Automated Impella Controller labeled as the following recall: Potential for Automated Impella Controller (AIC) purge pressure issues
Potential for Automated Impella Controller (AIC) purge pressure issues due to purge retainer failures.
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Class II · 1+ years ago
GE Medical Systems, LLC MAC VU360 Acquisition Trunk Cable and Module Holder recall: If a user incorrectly places the Acquisition Module into the Acquisition
If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the…
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Class II · 1+ years ago
Synthes Products LLC LOW Prof Lckng Screw, F/IM Nail 5.0MM / L recall: Although the etched length on the screw is correct
Although the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged…
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Class I · 1+ years ago
ICU Medical, Inc. IV Administration sets. 23" 150 mL Burette Set w/Clave, Luer Lock recall: IV Gravity burette administration set burette component is missing
IV Gravity burette administration set burette component is missing an internal shutoff valve intended to stop fluid flow, which if used may result in…
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Class II · 1+ years ago
Becton Dickinson & Co. BD EpiCenter Microbiology Data Management System recall: Product service credentials used by some BD technical support teams to access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Class II · 1+ years ago
Theken Companies LLC iNSitu Bipolar Hip System, Bipolar head implant Part ID recall: Downstream recall for RES 97605, BioPro femoral components. Product failed
Downstream recall for RES 97605, BioPro femoral components. Product failed transit testing. Impacted product may have potential issues with sterile…