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. 2,866 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,866 in last 12 months

Showing 1356113580 of 55,837 recalls

DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Akorn, Inc.

Recalled Item: Lidocaine Hydrochloride Oral Topical Solution Recalled by Akorn, Inc. Due to...

The Issue: Failed viscosity specification - product was below specificcation

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

Class III — Low RiskOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium & Hydrochlorothiazide Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Lidocaine 2.5% and Prilocaine 2.5% Cream Recalled by Teva Pharmaceuticals...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2022· Driscoll's Inc.

Recalled Item: Driscoll's Blackberries (Fresh) 12x6 oz Recalled by Driscoll's Inc. Due to...

The Issue: California Department of Pesticide Regulation detected the presence of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 14, 2022· Turbett Surgical, Inc.

Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Devices...

The Issue: Devices were subject to unapproved rework processes.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2022· Medtronic Inc

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Medtronic Inc Due to The pump...

The Issue: The pump may have a welding defect that can lead the pump to malfunction....

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 14, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 ToRC IgM Reagent Pack Recalled by Bio-Rad Laboratories, Inc....

The Issue: Performance concerns for the CMV IgM analyte. Analyte has demonstrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2022· Cerapedics, Inc.

Recalled Item: putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe Recalled by...

The Issue: Patient chart label contains incorrect Part Number and volume amount.

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

Class III — Low RiskOngoing
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Epinephrine Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Proventil HFA Recalled by Mckesson Medical-Surgical Inc. Corporate Office...

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Thrombin JMI Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Cefazolin for injection USP Recalled by Mckesson Medical-Surgical Inc....

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Duraclon (clonidine HCl injection Recalled by Mckesson Medical-Surgical Inc....

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: GlucaGen (glucagon) for injection Recalled by Mckesson Medical-Surgical Inc....

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Spinal Tray (A4058-25 Spinal Tray 25G Whitacre No Epinephrine) Recalled by...

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Dexmedetomidine HCL Single Dose Vial 200 mcg per 2 mL (100mcg/mL) Recalled...

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Intralipid (I.V. Fat emulsion) Recalled by Mckesson Medical-Surgical Inc....

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund