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. 2,754 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,754 in last 12 months

Showing 2184121860 of 55,837 recalls

Medical DeviceNovember 7, 2019· Neuronetrix Solutions, LLC dba Cognision

Recalled Item: Cognision Recalled by Neuronetrix Solutions, LLC dba Cognision Due to...

The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Abbott Gmbh & Co. KG

Recalled Item: ARCHITECT HAVAB-G Calibrator Recalled by Abbott Gmbh & Co. KG Due to Abbott...

The Issue: Abbott has identified that Calibrator lot 08219BE00 is potentially impacted...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...

The Issue: Beckman Coulter has become aware of an issue affecting Specific Gravity...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Howmedica Osteonics Corp.

Recalled Item: Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for Recalled...

The Issue: May have a missing locking wire causing delay in surgery while retrieving a...

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

Class II — Potential Health HazardOngoing
FoodNovember 7, 2019· Gold Standard Baking, Inc.

Recalled Item: Freshness Guaranteed Croissants in clear plastic 12oz clamshell Recalled by...

The Issue: Product is missing ingredient and nutrition label on bottom of clamshell...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 6, 2019· Qualigen Inc

Recalled Item: The FastPack System Comlete Immunoassay Kit Immunoassay for the Quantitative...

The Issue: The chemiluminescent immunoassay has been noted to have higher than expected...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2019· Allergan PLC

Recalled Item: Natrelle Silicone Filled Breast Implants for the following Styles and...

The Issue: The firm has became aware that 2D barcodes on breast implants and sizers may...

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2019· Allergan PLC

Recalled Item: Natrelle Saline-Filled Breast Implant Recalled by Allergan PLC Due to The...

The Issue: The firm has became aware that 2D barcodes on breast implants and sizers may...

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2019· Allergan PLC

Recalled Item: Natrelle Inspira Sillicone-Filled Breast Implants for the following Styles...

The Issue: The firm has became aware that 2D barcodes on breast implants and sizers may...

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2019· Allergan PLC

Recalled Item: NATRELLE Resterilizable Sizers for the styles and sizes: Style 15 Recalled...

The Issue: The firm has became aware that 2D barcodes on breast implants and sizers may...

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Color Cuff Disposable Tourniquet Cuff Recalled by Stryker Instruments Div....

The Issue: There is a potential for the cuff to leak air leading to a loss of vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Color Cuff Disposable Tourniquet Cuff Recalled by Stryker Instruments Div....

The Issue: There is a potential for the cuff to leak air leading to a loss of vascular...

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

Class II — Potential Health HazardOngoing
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Caspules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg Recalled by AuroMedics...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by AuroMedics Pharma LLC...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 300 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 5, 2019· Peekay International, Inc.

Recalled Item: Dry dates packaged under the following brands: Keshav Dry Yellow Dates...

The Issue: Product contains undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Avanos Medical, Inc.

Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...

The Issue: Avanos Medical has received reports stating that the central lumen of some 5...

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

Class II — Potential Health HazardOngoing