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. 1,132 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,132 in last 12 months

Showing 13561–13580 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 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· 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
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· 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· 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
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· 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 13, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...

The Issue: Siemens has become aware of three potential software issues with AXIOM...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge CM320 WUWD Series Washer Disinfector-For use as a multi-chamber...

The Issue: Verification of installation not documented or may be incomplete, could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - automated Recalled by Siemens Healthcare...

The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge CM320-2 CHAMBER WU Series Washer Disinfector- For Use as Recalled by...

The Issue: Verification of installation not documented or may be incomplete, could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Northgate Technologies, Inc.

Recalled Item: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe...

The Issue: Product labeled incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer - automated Recalled by Siemens Healthcare...

The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...

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

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

Recalled Item: Tetracaine Hydrochloride Ophthalmic Solution Recalled by Mckesson...

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: Glucagon Emergency Kit for Low Blood Sugar Recalled by Mckesson...

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: Geodon for injection (ziprasidone mesylate) Recalled by Mckesson...

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund