Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,747 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,747 in last 12 months

Showing 3478134800 of 48,330 recalls

Medical DeviceNovember 18, 2015· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...

The Issue: The treatment table positioning belt can slip gear positions, resulting in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Biomet, Inc.

Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...

The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...

The Issue: Some tubes were manufactured with the stopper not fully inserted into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...

The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen 5 Panel Dip Card w/Adult Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Smith & Nephew, Inc.

Recalled Item: BIRMINGHAM HIP RESURFACING MODULAR HEAD Recalled by Smith & Nephew, Inc. Due...

The Issue: The 16 devices distributed in the United States were incorrectly labeled as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: DrugSmart Cup 10 Recalled by Ameditech Inc Due to Ameditechs Drugs of Abuse...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: 11 Panel Card (OPI 300) w/Adult Recalled by Ameditech Inc Due to Ameditechs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ImmuTest Cup 7-panel w/ Adulteration Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen CLIA Waived Cup with 6 Drugs Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: Immutest 12 Panel Cup w/Adulteration Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: Immutest 10 Pnl Drug Screen Cup w/ Adult Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen Cup CLIA with 6 Panel Drug Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: 10-Panel Pipette Drug Screen Recalled by Ameditech Inc Due to Ameditechs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: iCup DX 6 Panel w/Adulterant Recalled by Ameditech Inc Due to Ameditechs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing