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. 1,032 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,032 in last 12 months

Showing 29121–29140 of 55,837 recalls

FoodMarch 28, 2018· Independent Nutrition, Inc.

Recalled Item: Ignite High Endurance Pre-Workout Supplement with Caffeine Recalled by...

The Issue: Ignite High Endurance Pre-Workout Supplement with Caffeine dietary...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2018· Independent Nutrition, Inc.

Recalled Item: Ignite High Endurance Pre-Workout Supplement CAFFEINE FREE Formula Recalled...

The Issue: Ignite High Endurance Pre-Workout Supplement Caffeine Free dietary...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2018· Independent Nutrition, Inc.

Recalled Item: Ignite High Endurance Pre-Workout Supplement Recalled by Independent...

The Issue: Ignite High Endurance Pre-Workout Supplement dietary supplement product is...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2018· Independent Nutrition, Inc.

Recalled Item: Enduravol Elite Pre-Workout Recalled by Independent Nutrition, Inc. Due to...

The Issue: Enduravol Elite Pre-Workout dietary supplement product is recalled because...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2018· Independent Nutrition, Inc.

Recalled Item: Ignite High Endurance Pre-Workout Supplement VANILLA Recalled by Independent...

The Issue: Ignite High Endurance Pre-Workout Supplement VANILLA dietary supplement...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 28, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The dose calculation accuracy may in some situations be less than expected....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Trilliant Surgical Ltd.

Recalled Item: Ratcheting Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due...

The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Trilliant Surgical Ltd.

Recalled Item: Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due to Firm is...

The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Teleflex Medical Europe Ltd

Recalled Item: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port Recalled...

The Issue: These one-way valves may disconnect at the joint between the two components...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.Via VB20A model 1049610 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Functionality in the report sections "Findings Information" and "Summary of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use...

The Issue: Urea Nitrogen reagent kit demonstrated an increased incidence of Calibration...

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

Class II — Potential Health HazardOngoing
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Linezolid Injection 600 mg per 300 mL (2 mg/mL) For Intravenous...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.82% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.54% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.75% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Lupin Cefdinir powder for Oral Suspension USP Recalled by Lupin...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2018· Bestco, Inc.

Recalled Item: Signature Care Calcium Chews Recalled by Bestco, Inc. Due to A packaging...

The Issue: A packaging revision and lack of revision to the corresponding packaging...

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

Class III — Low RiskOngoing
Refund