Product Recalls in Florida

Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,728 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,728 in last 12 months

Showing 2304123060 of 30,686 recalls

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: BZO Strip Dip Card (300ng/ml)* 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: ProScreen 6 Panel Dip Card Recalled by Ameditech Inc Due to Ameditechs Drugs...

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: DrugSmart 9 Test Cup (BUP) Recalled by Ameditech Inc Due to Ameditechs Drugs...

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 6 Drugs w/Adul 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: EDI BZO Uncut Sheet - Cup* Recalled by Ameditech Inc Due to Ameditechs Drugs...

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
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen 6 Panel Cassette w/Adult (AU) 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 5 Panel Dip Card Recalled by Ameditech Inc Due to Ameditechs Drugs...

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: 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: 6 Panel Cup Body and Lid w/Adult (AU) 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 10 Panel Cup Recalled by Ameditech Inc Due to Ameditechs Drugs of...

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· Nephron Pharmaceuticals Corp.

Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet HCU 30 Coolant Type R134A Filling weight 250 g Recalled by Maquet...

The Issue: Failure of the HEATER-COOLER UNIT (HCU 30) Type 2 power supply board. A drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Optima CL323i Product Usage: The angiographic X-ray systems...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Sterilmed, Inc. is voluntarily...

The Issue: Sterilmed, Inc. is voluntarily recalling all unexpired Reprocessed...

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

Class II — Potential Health HazardOngoing