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. 2,629 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,629 in last 12 months

Showing 4218142200 of 55,837 recalls

Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Lactate. Intended for use on COBAS INTEGRA 800 and 400 plus systems Recalled...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2)...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Triglycerides GPO. In vitro test for the quantitative determination of...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugMay 6, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium tablets Recalled by Dr. Reddy's...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2015· Golden Krust Caribbean Bakery, Inc.

Recalled Item: Golden Krust Caribbean JAMAICAN STYLE SHRIMP PATTIES Recalled by Golden...

The Issue: Golden Krust Caribbean Bakery & Grill has recalled their Jamaican Style...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 6, 2015· Golden Krust Caribbean Bakery, Inc.

Recalled Item: Golden Krust SOYA PATTIES Recalled by Golden Krust Caribbean Bakery, Inc....

The Issue: Golden Krust Caribbean Bakery & Grill has recalled their Jamaican Style...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 6, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: The Rapidlab 1265 system is a blood gas analyzer used Recalled by Siemens...

The Issue: D50 and D51 diagnostic error codes are not functional.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: The Rapidlab 1260 system is a blood gas analyzer used Recalled by Siemens...

The Issue: D50 and D51 Diagnostic error codes are not functional.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Custom Cardiovascular Procedure Kits Recalled by Terumo Cardiovascular...

The Issue: The Overpressure Safety Valve is not cleared with an indication for use on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2015· Smith & Nephew, Inc.

Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...

The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...

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

Class II — Potential Health HazardOngoing