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. 2,944 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,944 in last 12 months

Showing 161180 of 30,686 recalls

Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) ADMIT KIT Recalled by Medline Industries, LP...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) DRAPE PACK Recalled by Medline Industries, LP...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) DRAPE PACK-CHOICE Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT ACES INSERT PEG Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) ENDO KIT W/SYRINGE Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT UROLOGY SLING Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Surgical Packs: 1) PACK Recalled by Medline Industries, LP Due to...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) PICC LINE TRAY Recalled by Medline Industries,...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST Recalled by...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number:...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided)...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Olympus Corporation of the Americas

Recalled Item: Brand Name: Disposable Triple Lumen Sphincterotome Product Name: Disposable...

The Issue: Devices which did not undergo thermoforming could deform and lose performance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing