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. 2,723 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,723 in last 12 months

Showing 2598126000 of 55,837 recalls

Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· COVIDIEN LLC

Recalled Item: 8Fr SAFE GRAD CAT W/Valve (Argyle Suction Catheter Kits with Chimney Valve)...

The Issue: The product was released into commercial distribution while subject to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2018· Capintec Inc

Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...

The Issue: There is a potential for the spring arm failure as a result of a broken...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Baxter Healthcare Corporation

Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...

The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Stephanix

Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...

The Issue: The firm has detected a potential risk using the command. After releasing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2018· Virtual Imaging, Inc.

Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...

The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...

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

Class II — Potential Health HazardOngoing
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...

The Issue: Cross Contamination with Other Products

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits Recalled by Bound Tree...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Kit NOT FOR IV USE Recalled by Bound Tree Medical, LLC Due to...

The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2018· Boston Scientific Corporation

Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...

The Issue: Experienced accelerated battery depletion and a shortened replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2018· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Anti-HBe Reagent Pack Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to...

The Issue: The firm is extending their previous July 2018 recall to include additional...

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

Class II — Potential Health HazardOngoing