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. 2,923 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,923 in last 12 months

Showing 37613780 of 55,837 recalls

FoodDecember 30, 2024· V Chocolates, Inc

Recalled Item: Assorted Chocolate Caramels with kosher sea salt Recalled by V Chocolates,...

The Issue: Small pieces of plastic broken tray in the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP 30 mg Recalled by Rising Pharma...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine DR Capsules USP 60 mg Recalled by Rising Pharma Holding, Inc. Due...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP 20 mg Recalled by Rising Pharma...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 28, 2024· Neilmed Pharmaceuticals Inc

Recalled Item: NeiMed NasoGel for DRY NOSES UDI-DI/code: 00705928045309 SKU...

The Issue: Due to nasal spray stability failure for bioburden.

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

Class II — Potential Health HazardOngoing
DrugDecember 27, 2024· Eugia US LLC

Recalled Item: Progesterone Injection USP Recalled by Eugia US LLC Due to Presence of...

The Issue: Presence of Particulate Matter: A market complaint was received of a glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2024· Astellas Pharma US Inc.

Recalled Item: Prograf (tacrolimus) capsules Recalled by Astellas Pharma US Inc. Due to...

The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2024· Astellas Pharma US Inc.

Recalled Item: Astagraf XL (tacrolimus extended-release capsules) 0.5 mg Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2024· First Aid Beauty Ltd

Recalled Item: First Aid Beauty Ultra Repair Cream Recalled by First Aid Beauty Ltd Due to...

The Issue: CGMP Deviations; product intended for quarantine was inadvertently distributed

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2024· Viatris Inc

Recalled Item: Cardura XL (doxazosin) extended release tablets 8 mg Recalled by Viatris Inc...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2024· Viatris Inc

Recalled Item: Cardura XL (doxazosin) extended release tablets 4 mg Recalled by Viatris Inc...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast SlimFit Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Recalled by Hollister Incorporated Due to Hollister received...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Guard Select Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Hollister Incorporated

Recalled Item: AnchorFast Guard Recalled by Hollister Incorporated Due to Hollister...

The Issue: Hollister received reports of decreased skin barrier wear time which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Oxoid Limited

Recalled Item: Lev5 Recalled by Oxoid Limited Due to Mislabeling

The Issue: Mislabeling; Levofloxacin Antimicrobial susceptibility disc packaging may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Accuray Incorporated

Recalled Item: CyberKnife Treatment Delivery System Recalled by Accuray Incorporated Due to...

The Issue: Snap rings may become partially or completed detached from the shafts within...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ARTERIAL LINE PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Certain lots Sterile Infusion Catheters which were mislabeled as having a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION Infusion Catheter Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Certain lots Sterile Infusion Catheters which were mislabeled as having a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2024· Percussionaire Corporation

Recalled Item: VDR4 Phasitron Breathing Circuit Models that contain the venturi component:...

The Issue: Due to internal venturi component getting transiently stuck in the forward...

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

Class I — Serious Health HazardOngoing