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. 2,911 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,911 in last 12 months

Showing 55015520 of 30,686 recalls

Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· CardioQuip, LLC

Recalled Item: CardioQuip Modular Cooler-Heater Recalled by CardioQuip, LLC Due to There is...

The Issue: There is a potential for the heating-chamber to malfunction resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: KWIKSTIK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform 100-240V- 50/60Hz 1440w Recalled by AURIS HEALTH INC Due to...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS icono (ceiling configuration) Recalled by Siemens Medical Solutions...

The Issue: Potential hardware issue for ARTIS icono ceiling system: collision sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray TORCH . HTFA-ASY-0104 is the BIOFIRE TORCH Base Recalled by...

The Issue: Due to an increased risk of degradation of the power entry switch resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...

The Issue: Routine quality control testing of affected blood culture identification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· Aizu Olympus Co., Ltd.

Recalled Item: GIF-HQ190 Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...

The Issue: Specific devices may have an improperly repaired light guide connector due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Nurse Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Nursing Skills kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2023· Zimmer Biomet Spine Inc.

Recalled Item: Vitality Polyaxial Screw Recalled by Zimmer Biomet Spine Inc. Due to Spinal...

The Issue: Spinal fixation system 7.5mmx 50mm screws are packaged with the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· Aizu Olympus Co., Ltd.

Recalled Item: PCF-H190L Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...

The Issue: Specific devices may have an improperly repaired light guide connector due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· Aizu Olympus Co., Ltd.

Recalled Item: GIF-H190 Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may have...

The Issue: Specific devices may have an improperly repaired light guide connector due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· Aizu Olympus Co., Ltd.

Recalled Item: CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE Recalled by Aizu Olympus Co., Ltd....

The Issue: Specific devices may have an improperly repaired light guide connector due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· Aizu Olympus Co., Ltd.

Recalled Item: PCF-H190DL Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...

The Issue: Specific devices may have an improperly repaired light guide connector due...

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

Class II — Potential Health HazardOngoing