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. 2,939 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,939 in last 12 months

Showing 29412960 of 55,837 recalls

Medical DeviceMarch 28, 2025· Micro-X Ltd.

Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...

The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2025· Micro-X Ltd.

Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...

The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2025· Stryker GmbH

Recalled Item: Guide Wire with Ruler Tube 3x800 mm DIA Recalled by Stryker GmbH Due to The...

The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2025· Stryker GmbH

Recalled Item: Guide Wire with Ruler Tube 3x1000 mm DIA Recalled by Stryker GmbH Due to The...

The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: GALT Guidewire Guidewires are intended for use in Recalled by Galt Medical...

The Issue: Due to a potential open seal in the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: B Braun Interventional Coaxial Dilator Recalled by Galt Medical Corporation...

The Issue: Due to a potential open seal in the sterile barrier packaging .

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: B Braun Interventional ELITE HV Hemostasis Valve Introducer System by Galt...

The Issue: Due to a potential open seal in the sterile barrier packaging .

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Bausch & Lomb Surgical, Inc.

Recalled Item: Intraocular Lens. enVista Envy IOL Recalled by Bausch & Lomb Surgical, Inc....

The Issue: In response to an increased number of reports of toxic anterior segment...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: Introducer Kit- Tearaway MicroSlide Recalled by Galt Medical Corporation Due...

The Issue: Due to a potential open seal in the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: Introducer Needle These needles are used for the Recalled by Galt Medical...

The Issue: Due to a potential open seal in the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: Introducer Kit- Coaxial Dilator Recalled by Galt Medical Corporation Due to...

The Issue: Due to a potential open seal in the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· Bausch & Lomb Surgical, Inc.

Recalled Item: Intraocular lens. enVista Monofocal IOL Recalled by Bausch & Lomb Surgical,...

The Issue: In response to an increased number of reports of toxic anterior segment...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: GALT Centeze Catheter DRC-002-06 The Centeze is intended Recalled by Galt...

The Issue: Due to a potential open seal in the sterile barrier packaging .

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· IHB OPERATIONS B.V.

Recalled Item: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount Recalled by IHB OPERATIONS...

The Issue: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does...

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

Class II — Potential Health HazardOngoing
FoodMarch 26, 2025· The Truck Farm, LLC

Recalled Item: Desert Farms Jalapeno Mustard. Caution to after opening. The Recalled by The...

The Issue: The product is in violation for not having an approved filed process and for...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 26, 2025· Frito-Lay, Inc. Headquarters

Recalled Item: Tostitos Cantina Traditional Yellow Corn Tortilla Chips. Net Wt. 13oz....

The Issue: Undeclared allergen (milk).

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 26, 2025· Chattem Inc

Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations; detection of...

The Issue: CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 25, 2025· MTN OPS, LLC

Recalled Item: MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement Recalled by MTN...

The Issue: Undeclared soy flour

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 25, 2025· OLD WORLD SPICES & SEASONING, INC

Recalled Item: Lillie's Q Buffalo Wing Sauce. Net wt. 13.5 oz Recalled by OLD WORLD SPICES...

The Issue: Undeclared allergen (milk not listed as sub ingredient of butter). Milk also...

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

Class II — Potential Health HazardOngoing
Refund