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. 2,698 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,698 in last 12 months

Showing 3356133580 of 55,837 recalls

DrugMarch 17, 2017· Shire

Recalled Item: Kalbitor (ecallantide) Recalled by Shire Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2017· Akorn, Inc.

Recalled Item: LATANOPROST OPHTHALMIC SOLUTION Recalled by Akorn, Inc. Due to Lack of...

The Issue: Lack of assurance of sterility: product was found to be empty, under-filled,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2017· Allergan Sales, LLC

Recalled Item: Lumigan (bimatoprost ophthalmic solution) 0.01% Recalled by Allergan Sales,...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 16, 2017· Fresenius Kabi USA, LLC

Recalled Item: Fluphenazine Decanoate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Ortho Basic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Zimmer Biomet Spine, Inc

Recalled Item: Altius M-INI OCT Posterior Spinal Fixation System Recalled by Zimmer Biomet...

The Issue: Zimmer Biomet is recalling the Altius M-INI OCT Posterior Spinal Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes Recalled...

The Issue: BD is initiating this product correction of multiple lots of BD Vacutainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Dicken Eye Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: PRK Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Vitrectomy Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Ophthalmic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Dr. Wischmeier Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Vitrectomy Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Setup Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Lasik Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: ENT Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Kit - Dr. Slingsby Recalled by Windstone Medical Packaging, Inc....

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Minor Operation Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing