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. 2,723 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,723 in last 12 months

Showing 2532125340 of 55,837 recalls

Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2019· Bioventus, LLC

Recalled Item: BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device...

The Issue: The firm became aware of the potential for the products' sterile pouch to be...

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

Class II — Potential Health HazardOngoing
FoodFebruary 13, 2019· Friendly Fruit Market dba Sid Wainer & Son

Recalled Item: JANSAL VALLEY DUKKAH NET WT 2.5 oz. (71 G). The Recalled by Friendly Fruit...

The Issue: Customer found piece of glass in the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lovastatin Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2019· Perrigo New York, Inc.

Recalled Item: Ciclopirox shampoo 1% Recalled by Perrigo New York, Inc. Due to Failed...

The Issue: Failed Degradation/Impurities Specifications: Out of specification related...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Optima PET/CT 560 Recalled by GE Healthcare, LLC Due to GE Healthcare PET/CT...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 610 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e500 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e700 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· O-Two Medical Technologies, Inc.

Recalled Item: e600 Automatic Transport Ventilator Recalled by O-Two Medical Technologies,...

The Issue: There is a potential for the unit to catch fire due to one of the screen...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml DR Product Usage: The systems are intended for Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery PET/CT 710 Product Usage: The systems are intended for Recalled by...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery Ml Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2019· GE Healthcare, LLC

Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...

The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

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

Class II — Potential Health HazardOngoing
FoodFebruary 12, 2019· King Orchards

Recalled Item: Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual...

The Issue: Incorrect quantity of sugar listed in Nutrition Facts. Label states 1g sugar...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...

The Issue: Incorrect needle length and gage.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Fenwal Inc

Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...

The Issue: The optional Vacuum Unit may stop working and display the failure message...

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

Class II — Potential Health HazardOngoing