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 2668126700 of 55,837 recalls

Medical DeviceAugust 24, 2018· ShinChang Medical Co., Ltd.

Recalled Item: Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2 Recalled by...

The Issue: Defect consists of a small crack in the top end of the barrel near the needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco Sodium Pyruvate (100 mM) SKU 11360070 Recalled by Life Technologies,...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2018· Life Technologies, Corp.

Recalled Item: Gibco DPBS Recalled by Life Technologies, Corp. Due to Leaky bottles due to...

The Issue: Leaky bottles due to a defect in the bottle cap compromising the sterility...

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

Class II — Potential Health HazardOngoing
DrugAugust 24, 2018· LGM Pharma LLC

Recalled Item: Thyroid Powder Recalled by LGM Pharma LLC Due to CGMP Deviations: Thyroid...

The Issue: CGMP Deviations: Thyroid Powder has inconsistent levels of the active...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2018· Akorn, Inc.

Recalled Item: Ethosuximide Capsules Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2018· Hellolife

Recalled Item: Thyroveev Recalled by Hellolife Due to Microbial Contamination of Non...

The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2018· Hellolife

Recalled Item: Compulsin Recalled by Hellolife Due to Microbial Contamination of Non...

The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2018· Hellolife

Recalled Item: Neuroveen Recalled by Hellolife Due to Microbial Contamination of Non...

The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2018· Hellolife

Recalled Item: Respitrol Recalled by Hellolife Due to Microbial Contamination of Non...

The Issue: Microbial Contamination of Non Sterile Products; Products contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2018· LUPIN SOMERSET

Recalled Item: Morphine Sulfate Extended-Release Tablets Recalled by LUPIN SOMERSET Due to...

The Issue: Failed Impurities/Degradation Specifications: Morphine Sulfate Extended...

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

Class III — Low RiskOngoing
Refund
DrugAugust 23, 2018· Pfizer Global Supply

Recalled Item: Children s Advil Suspension Ibuprofen Oral Suspension Recalled by Pfizer...

The Issue: Labeling Error: Not elsewhere classified. product has a dosage cup marked in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2018· Becton Dickinson & Company

Recalled Item: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva...

The Issue: One lot of the specified needles is not performing as intended due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2018· Tosoh Bioscience Inc

Recalled Item: AIA-360 Analyzer Recalled by Tosoh Bioscience Inc Due to The firm has...

The Issue: The firm has implemented new product labeling changes for the Tosoh AIA-360...

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

Class II — Potential Health HazardOngoing
FoodAugust 23, 2018· Dewey's Bakery, Inc dba Salem Baking Company

Recalled Item: Dewey's BAKERY Soft Baked TRIPLE CHOCOLATE BROWNIE COOKIES NET WT. Recalled...

The Issue: The firm was notified by a customer that mold was in the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 12mm SpinDown Clamp Recalled by Zimmer...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp :...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...

The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

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

Class II — Potential Health HazardOngoing