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. 1,075 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,075 in last 12 months

Showing 18721–18740 of 55,837 recalls

Medical DeviceNovember 3, 2020· GA HEALTH COMPANY LIMITED

Recalled Item: STOPCON Suction Valve-Suction Valve for GI-Endoscope DISTRIBUTED BY: KEY...

The Issue: Suction button is reported sticky and/or broken during or after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2020· GA HEALTH COMPANY LIMITED

Recalled Item: STOPCON Disposable Valves Set-Single Use Valves...

The Issue: Suction button is reported sticky and/or broken during or after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2020· GA HEALTH COMPANY LIMITED

Recalled Item: Andorate Disposable Endoscope Valves Set-5-piece Valve Recalled by GA HEALTH...

The Issue: Suction button is reported sticky and/or broken during or after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2020· Kowa Optimed Inc

Recalled Item: Kowa VK-2s software Version 10.0.4.0 Recalled by Kowa Optimed Inc Due to It...

The Issue: It has been determined that the software distributed with the retinal camera...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2020· GA HEALTH COMPANY LIMITED

Recalled Item: ScopeValet Guardian Disposable Endoscope Valves Set Distributed By Ruhof...

The Issue: Suction button is reported sticky and/or broken during or after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2020· K2M, Inc

Recalled Item: Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Recalled...

The Issue: Shafts do not pass through the inner cannula of the Anti-Torque Alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2020· NEOSTEO

Recalled Item: Cannulated graduated drill bit 1.9 mm diameter Recalled by NEOSTEO Due to...

The Issue: Traces of corrosion on the laser marking was detected on cannulated...

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

Class II — Potential Health HazardOngoing
DrugNovember 3, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Sodium Chloride Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Failed pH Specifications: Out of Specification pH Test Results were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 3, 2020· Teligent Pharma, Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Teligent Pharma, Inc. Due to...

The Issue: Subpotent Drug: One lot of Triamcinolone Acetonide Lotion, 0.025% 60 mL.does...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage:...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage:...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: MassChrom Amino Acid Analysis Plasma Control Level I Recalled by...

The Issue: Products do not meet stability criteria and may impact results.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: 3PLUS1 Multilevel Plasma Calibrator Set Recalled by Chromsystems Instruments...

The Issue: Products do not meet stability criteria and may impact results.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage:...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage:...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage:...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage:...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V680 Ventilator Part Number 850011 - Product Usage:...

The Issue: Potential issues with ventilator navigation ring interface and liquid...

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

Class II — Potential Health HazardOngoing