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. 2,710 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,710 in last 12 months

Showing 3006130080 of 55,837 recalls

Medical DeviceDecember 5, 2017· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to An accessory...

The Issue: An accessory (range shifter, ridge filter&) can be improperly inserted in...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Enoxaparin Sodium Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. A single syringe labeled as 150...

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

Class III — Low RiskOngoing
Refund
FoodDecember 5, 2017· Creative Contract Packaging Corporation, LLC

Recalled Item: HERB-OX Beef Flavor Granulated Bouillon Recalled by Creative Contract...

The Issue: Creative Contract Packaging LLC is voluntarily recalling two code dates of...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 5, 2017· Aldi Inc

Recalled Item: Choceur Dark Chocolate Bars Recalled by Aldi Inc Due to Undeclared Treenut

The Issue: ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 4, 2017· McCain Foods USA

Recalled Item: Publix brand Recalled by McCain Foods USA Due to Foreign Object Contamination

The Issue: Publix brand Southern Style Diced Hash Brown Potatoes, net wt. 32 oz....

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2017· ALLERGAN

Recalled Item: Viokace (pancrelipase) tablets Recalled by ALLERGAN Due to Subpotent Drug:...

The Issue: Subpotent Drug: One lot of Viokace is being recalled since product stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2017· AuroMedics Pharma LLC

Recalled Item: Pantoprazole Sodium for Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Beckman Coulter Inc.

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

The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Cellavision AB

Recalled Item: CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the Recalled by...

The Issue: A software malfunction was found where WBC, RBC and PLT comments added after...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Smiths Medical ASD Inc.

Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...

The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Smiths Medical ASD Inc.

Recalled Item: Power PORT-A-CATH II Recalled by Smiths Medical ASD Inc. Due to Certain...

The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2017· ProSun International, LLC

Recalled Item: Sundream 12 V tanning bed Recalled by ProSun International, LLC Due to The...

The Issue: The 30 minute maximum tanning time has been reduced to 20 minutes.

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

Class II — Potential Health HazardOngoing