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. 1,921 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,921 in last 12 months

Showing 3216132180 of 55,837 recalls

Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
DrugJune 5, 2017· Bristol-myers Squibb Company

Recalled Item: EliquisTablets 5mg Recalled by Bristol-myers Squibb Company Due to Labeling:...

The Issue: Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 5, 2017· Apothecary By Design

Recalled Item: Progesterone Injection in Olive Oil With Benzyl Alcohol 10% Recalled by...

The Issue: Lack of Processing Controls: The metal container closure adheres to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2017· G & W Laboratories, Inc.

Recalled Item: G & W Clobetasol Propionate Ointment 0.05% Recalled by G & W Laboratories,...

The Issue: Failed impurities/degradation specifications: This product is being recalled...

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

Class III — Low RiskOngoing
Refund
FoodJune 2, 2017· Star Snacks Co., Llc.

Recalled Item: Southern Grove Cashew Halves & Pieces with Sea Salt Recalled by Star Snacks...

The Issue: The firm received notification from a consumer finding a glass fragment in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· Sterilmed Inc

Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...

The Issue: Inadequate seal due to lack of adhesive glue

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· C.R. Bard, Inc.

Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...

The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Arrow International Inc

Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...

The Issue: There is a possibility that the finished good kits may contain 5 Fr...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans SFILL 360 Recalled by Shippert Medical Technologies Due to Seal...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 250 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Arrow International Inc

Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...

The Issue: There is a possibility that the finished good kits may contain 5 Fr...

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

Class II — Potential Health HazardOngoing