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. 2,706 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,706 in last 12 months

Showing 3236132380 of 55,837 recalls

Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima CT580 Recalled by GE Healthcare, LLC Due to It was...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima CT520 X-ray system Recalled by GE Healthcare, LLC Due...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare LightSpeed VCT X-ray system Recalled by GE Healthcare, LLC Due...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery IQ X-ray system Recalled by GE Healthcare, LLC Due...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery NM/CT 670. 670 Pro Recalled by GE Healthcare, LLC...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery Ml DR X-ray system Recalled by GE Healthcare, LLC...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· Neusoft Medical Systems Co., Ltd.

Recalled Item: Neusoft Medical NeuViz 64 Multi-slice CT Scanner System Recalled by Neusoft...

The Issue: Software defect

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare lnnova IGS 540 ACT X-ray system Recalled by GE Healthcare, LLC...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare BrightSpeed X-ray system Recalled by GE Healthcare, LLC Due to...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima CT540 X-ray system Recalled by GE Healthcare, LLC Due...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery PET/CT 600 Recalled by GE Healthcare, LLC Due to It...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· Neusoft Medical Systems Co., Ltd.

Recalled Item: Neusoft NeuViz 128 Multi-slice CT Scanner System Product Usage: The Recalled...

The Issue: Software defect

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

Class II — Potential Health HazardOngoing
DrugMay 19, 2017· DYNAMIC TECHNICAL FORMULATIONS

Recalled Item: Biotech Underground Tri-Ton Hardcore Formula capsules Recalled by DYNAMIC...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable Recalled by...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable Recalled by...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: morphine sulfate in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable Recalled...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· Hospira Inc., A Pfizer Company

Recalled Item: Levophed norepinephrine bitartrate Recalled by Hospira Inc., A Pfizer...

The Issue: GMP Deviation; A foreign stopper was observed during packaging of a lot of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund