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 32613280 of 55,837 recalls

Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid MR IMRIS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Operating table column TS7500 MOBIUS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Progressa Bed Surfaces Recalled by Baxter Healthcare Corporation Due to The...

The Issue: The air bladders inside the mattress may move out of position when the head...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (FC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid Plus (SC) Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Floor mounting column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Floor mounting column TS 7500 U Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Mobile column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2025· Imprimis NJOF, LLC

Recalled Item: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic...

The Issue: Sub-Potent Drug: The stability batch showed a subpotent result, which does...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 24, 2025· Denison Pharmaceuticals, LLC

Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...

The Issue: Chemical Contamination: Presence of benzene.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
FoodFebruary 21, 2025· Shearer's Foods, LLC

Recalled Item: 1.) Market Pantry Soup & Oyster Crackers Recalled by Shearer's Foods, LLC...

The Issue: Potential foreign material (stainless steel wire)

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 21, 2025· DANONE WAVE

Recalled Item: HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) Recalled by...

The Issue: The firm received complaints of spoilage and illness with the use of the...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 21, 2025· DANONE WAVE

Recalled Item: CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL...

The Issue: The firm received complaints of spoilage and illness with the use of the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 21, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline medical procedure kits, containing Medtronic Aortic Root Cannula

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

Class I — Serious Health HazardOngoing