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. 2,710 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,710 in last 12 months

Showing 3124131260 of 55,837 recalls

FoodJuly 21, 2017· Bush Brothers & Co

Recalled Item: BUSH'S BEST¿ Brown Sugar Hickory SWEET HICKORY SAUCE WITH BROWN Recalled by...

The Issue: During an FDA inspection the firm was informed that cans may have defective...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 21, 2017· Professional Complementary Health Formulas, LLC

Recalled Item: Professional Formulas Sublinqual B12 High-Potency dietary supplement...

The Issue: Sublinqual B12 tablets are recalled because the ingredients statement...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 21, 2017· Howmedica Osteonics Corp.

Recalled Item: Accolade and Restoration hip product Recalled by Howmedica Osteonics Corp....

The Issue: Inner and outer sterile barriers not fully sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Howmedica Osteonics Corp.

Recalled Item: Accolade and Restoration hip product Recalled by Howmedica Osteonics Corp....

The Issue: Inner and outer sterile barriers not fully sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Swish Duo-Grip Healing Collar Recalled by Implant Direct...

The Issue: The Swish Duo-Grip Healing Collar part number 9048-13H (4.8mm) package...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2017· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: FUJINON ED-530XT. This device is intended for the visualization of Recalled...

The Issue: An update to the design and labeling was implemented to help reduce patient...

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

Class II — Potential Health HazardOngoing
FoodJuly 20, 2017· Grandma's Herbs

Recalled Item: "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT Recalled by...

The Issue: Grandmas Herbs Cholesterol has undeclared soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 20, 2017· Beckman Coulter Inc.

Recalled Item: Sekisui Diagnostics Sekure Chemistry Acetaminophen L3K Recalled by Beckman...

The Issue: Reagent carryover from Sekisui ACTH when utilized on the BEC AU 680 analyzer...

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

Class II — Potential Health HazardOngoing
DrugJuly 19, 2017· AVKARE Inc.

Recalled Item: Voriconazole Tablets Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out of specification for a...

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

Class III — Low RiskOngoing
Refund
FoodJuly 19, 2017· TRULY GOOD FOODS

Recalled Item: Pumpkin Seeds Recalled by TRULY GOOD FOODS Due to Undeclared Allergen

The Issue: Undeclared allergen Tree Nuts: Blackened Seasoned Pumpkin Seeds mixed up...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 19, 2017· Genicon, Inc.

Recalled Item: GENICON EZEE Retrieval Recalled by Genicon, Inc. Due to Plastic handle is...

The Issue: Plastic handle is breaking off of shaft inhibiting proper removal per...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Kamiya Biomedical Company, LLC

Recalled Item: K-Assay(R) Multi-Analyte Calibrator Recalled by Kamiya Biomedical Company,...

The Issue: The AlAT calibrator values in the package insert for the Multi-Analyte...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...

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

Class II — Potential Health HazardOngoing