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. 1,071 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,071 in last 12 months

Showing 22701–22720 of 55,837 recalls

Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...

The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...

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

Class II — Potential Health HazardOngoing
FoodAugust 28, 2019· Jivan Shakti Inc.

Recalled Item: Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C....

The Issue: Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis...

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

Class III — Low RiskOngoing
Refund
DrugAugust 28, 2019· AVKARE Inc.

Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...

The Issue: Failed Stability Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2019· American Health Packaging

Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 27, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Drill Sleeve Guides Recalled by Ad-Tech Medical Instrument...

The Issue: The inner diameter of the drill sleeve guide raw material was found to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE Recalled by Karl Storz Endoscopy...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to During a...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz Recalled by Karl Storz Endoscopy Due to During a complaint...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2019· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...

The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2019· LivaNova Deutschland GmbH

Recalled Item: Control Panel 60-02-15: LivaNova SCP Pump Control Panel. Recalled by...

The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2019· LivaNova Deutschland GmbH

Recalled Item: Control Panel 60-02-50: LivaNova SCP Pump Control Panel Recalled by LivaNova...

The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...

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

Class II — Potential Health HazardOngoing
FoodAugust 26, 2019· Hometown Food Company

Recalled Item: Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix Recalled by...

The Issue: Product tested positive for gluten but is labeled as Gluten free

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 26, 2019· Natures One Inc

Recalled Item: PediaSmart Organic Soy Vanilla Beverage Mix Recalled by Natures One Inc Due...

The Issue: Undeclared milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2019· Tuscano and Delucia Group (DBA Entropic Labs)

Recalled Item: Entropic Labs SARM RAD-140 Recalled by Tuscano and Delucia Group (DBA...

The Issue: Marketed Without An Approved NDA/ANDA: product contains Selective Androgen...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochrloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Wal-Fex (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund