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. 1,206 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,206 in last 12 months

Showing 1621–1640 of 55,837 recalls

DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot Upgrade. Model Number: 10684334. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396 Recalled by...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Biograph mMR. Model Number: 10433372. Recalled by Siemens Medical Solutions...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma. Model Number: 10849582. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Lantiseptic Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: GelRite Instant Hand Sanitizer Recalled by DermaRite Industries, LLC Due to...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Hand-E-Foam Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: UltraSure Anti-Perspirant & Deodorant Recalled by DermaRite Industries, LLC...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Renew Skin Repair Cream Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: McKesson Skin Protectant Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: PeriGuard Ointment Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: Renew PeriProtect Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaMed Ointment Recalled by DermaRite Industries, LLC Due to CGMP...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2025· DermaRite Industries, LLC

Recalled Item: DermaFungal Recalled by DermaRite Industries, LLC Due to CGMP Deviation;...

The Issue: CGMP Deviation; manufactured at the same facility where other products and...

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

Class II — Potential Health HazardOngoing
Refund