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. 2,739 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,739 in last 12 months

Showing 2258122600 of 55,837 recalls

DrugSeptember 12, 2019· Pfizer Inc.

Recalled Item: ethosuximide capsules Recalled by Pfizer Inc. Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2019· Merit Medical Systems, Inc.

Recalled Item: Custom Sheath Introducer Kit - Product Usage: intended Recalled by Merit...

The Issue: labeling error: Due to a manufacturing issue, product package was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Olympus Corporation of the Americas

Recalled Item: Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System -...

The Issue: Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Integra LifeSciences Corp.

Recalled Item: Cerelink ICP Monitor Recalled by Integra LifeSciences Corp. Due to There is...

The Issue: There is a potential for a progressive decline in observed ICP readings of...

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

Class II — Potential Health HazardOngoing
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Fresh Grab brand Ham & Cheese Recalled by Lipari Foods Operating Company,...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo and Fresh Grab brands Egg Salad Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Fresh Grab brand Turkey No Cheese Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo and Fresh Grab brands Chicken Salad Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo and Fresh Grab brands Tuna Salad Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo brand Bologna & Cheese Wedge Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2019· Mizuho America, Inc.

Recalled Item: Microsurgical Operating Room Tables Recalled by Mizuho America, Inc. Due to...

The Issue: Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Mizuho America, Inc.

Recalled Item: Microsurgical Operating Room Tables Recalled by Mizuho America, Inc. Due to...

The Issue: Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M1356A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Tocotransducer (Nautilus) 2264LAX Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco MP Transducer (M2734B) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V60 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco M2734A Recalled by Pacific Medical Group Inc. Due to Fetal/maternal...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-Touch Screen Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing