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. 1,180 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,180 in last 12 months

Showing 2581–2600 of 30,686 recalls

Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Ltd.

Recalled Item: Eclipse Mini The Eclipse MINI Model 98900 is Recalled by Spacelabs...

The Issue: Due to a manufacturing error the incorrect device serial number was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver with Software Recalled by Spacelabs Healthcare,...

The Issue: Telemetry receivers with affected software versions may experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - Donaldson - Blue Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 9mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - Donaldson - Double - Blue Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 12mm - Double - Silicone Recalled by...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2024· Adept Medical Ltd

Recalled Item: Otological Ventilation Tube - T-Tube 6mm - Silicone Recalled by Adept...

The Issue: Lack of 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2024· Nipro Renal Soultions USA, Corporation

Recalled Item: Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25...

The Issue: The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.

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

Class II — Potential Health HazardOngoing