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. 2,940 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,940 in last 12 months

Showing 741760 of 55,837 recalls

Medical DeviceNovember 10, 2025· Beckman Coulter, Inc.

Recalled Item: COULTER DxH Diluent Recalled by Beckman Coulter, Inc. Due to Due to specific...

The Issue: Due to specific lots of diluents contributing to elevated platelet Daily...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 60 Recalled by Draeger, Inc. Due to Multiple complaints were...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 45 Recalled by Draeger, Inc. Due to Multiple complaints were...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 10, 2025· Draeger, Inc.

Recalled Item: ErgoStar CM 55 Recalled by Draeger, Inc. Due to Multiple complaints were...

The Issue: Multiple complaints were reported in which cracks formed in the hose of...

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

Class I — Serious Health HazardOngoing
FoodNovember 8, 2025· ByHeart, INC.

Recalled Item: 1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams Recalled by...

The Issue: Contaminated with Clostridium botulinum

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 8, 2025· Pacific Seafood - Portland, LLC

Recalled Item: Pacific Seafood Raw Blackened Shrimp Peeled & Deveined Tail-Off Recalled by...

The Issue: Undeclared Sulfite. Shrimp may contain 3.4mg Sulfur Dioxide per serving and...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 7, 2025· Intuitive Surgical, Inc.

Recalled Item: Brand Name: Da Vinci Product Name: da Vinci X Recalled by Intuitive...

The Issue: Due to a software implementation error that allowed instruments arms failing...

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

Class II — Potential Health HazardOngoing
FoodNovember 7, 2025· Costco Wholesale Corporation

Recalled Item: Costco Item# 11444 Kirkland Signature Chicken Sandwich with Caesar Salad...

The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Chicken Sandwich w/...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 7, 2025· Costco Wholesale Corporation

Recalled Item: Costco Item# 19927 Kirkland Signature Caesar Salad Recalled by Costco...

The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Caesar Salad may contain...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Carton label: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA, Inc...

The Issue: Defective Container - A defect in the side-seal which allows leakage of product.

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 7, 2025· Beckman Coulter, Inc.

Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...

The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...

The Issue: Due to a number of modules flashed with a date and time associated with the...

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

Class II — Potential Health HazardOngoing
FoodNovember 6, 2025· VENTURA FOODS LLC

Recalled Item: Publix Deli Carolina-Style Mustard BBQ Sauce Recalled by VENTURA FOODS LLC...

The Issue: foreign objects (black plastic planting material) in granulated onion

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 6, 2025· VENTURA FOODS LLC

Recalled Item: Italian Salad Dressing Recalled by VENTURA FOODS LLC Due to Foreign Object...

The Issue: foreign objects (black plastic planting material) in granulated onion

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2025· Fresenius Kabi USA, LLC

Recalled Item: Famotidine Injection Recalled by Fresenius Kabi USA, LLC Due to Microbial...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: Bard InLay Optima Size: 6 Fr. x 14 cm Recalled by C.R. Bard Inc Due to...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm Recalled by C.R....

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· Bard Peripheral Vascular Inc

Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Bard Peripheral...

The Issue: Acute drainage catheters, indicated for use in removing fluid during acute...

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

Class II — Potential Health HazardOngoing