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. 2,654 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,654 in last 12 months

Showing 4144141460 of 55,837 recalls

Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Nobel Biocare Usa Llc

Recalled Item: Abutment Retrieval Instrument Zirconia CC RP/WP Recalled by Nobel Biocare...

The Issue: One dimension of the affected instrument is incorrect. Therefore this...

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

Class II — Potential Health HazardOngoing
FoodJune 19, 2015· Niagara Bottling, LLC

Recalled Item: Acadia Natural Spring Water Recalled by Niagara Bottling, LLC Due to...

The Issue: Source Spring Water was analyzed and found positive for E. coli and total...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJune 19, 2015· Project 7

Recalled Item: Sour Caramel Apple Chewing Recalled by Project 7 Due to Undeclared Milk

The Issue: Project 7 is recalling all lots of Sour Caramel Apple Chewing Gum because...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2015· CooperSurgical, Inc.

Recalled Item: Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Recalled...

The Issue: Incorrect expiration date on outer carton kit label

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

Class II — Potential Health HazardOngoing
DrugJune 18, 2015· Qualitest Pharmaceuticals

Recalled Item: Disulfiram tablets Recalled by Qualitest Pharmaceuticals Due to Failed...

The Issue: Failed Dissolution Specifications: During routine stability testing at the...

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

Class III — Low RiskOngoing
Refund
FoodJune 18, 2015· Sysco Corporation

Recalled Item: Sysco International Whole Segments Mandarin Oranges In Light Syrup Net...

The Issue: Product tested positive for Carbendazim.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2015· ConMed Corporation

Recalled Item: Arthroscopic Energy 50¿ Probe with Suction Recalled by ConMed Corporation...

The Issue: Probe programming error. The incorrect program can generate more heat at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2015· Acon Laboratories, Inc.

Recalled Item: Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Recalled by Acon...

The Issue: Acon Laboratories, Inc. is recalling Mission Breath Alcohol Detector due to...

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

Class III — Low RiskOngoing
Medical DeviceJune 17, 2015· Philips Electronics North America Corporation

Recalled Item: Invivo Expression MRI Patient Monitoring System. Recalled by Philips...

The Issue: The device's labeling inaccurately indicates Endotracheal as a body...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2015· Symmetry Surgical, Inc.

Recalled Item: SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP Recalled by Symmetry Surgical, Inc....

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2015· Intuitive Surgical, Inc.

Recalled Item: INSTRUMENT ARM DRAPE Recalled by Intuitive Surgical, Inc. Due to Field...

The Issue: Field Safety Notification to advise of an issue that may occur involving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2015· Nidek Inc

Recalled Item: OPD-Scan III Power/Corneal Analyzer Opthalmic Software versions 1.00.08...

The Issue: Software bug was found where there was no difference in Total and Corneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2015· Abbott Point Of Care Inc.

Recalled Item: i-Stat PT/INR Cartridges List number 03P89-24 The cartridges are packaged...

The Issue: Certain lots of PT/INR cartridges may generate a higher than typical number...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2015· Mermaid Medical A/S

Recalled Item: Mermaid Medical M-Biopsy Coaxial Introducer Needle Recalled by Mermaid...

The Issue: Mermaid Medical A/S is recalling some of their M-Biopsy Coaxial Introducer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2015· Sorin Group USA, Inc.

Recalled Item: Sorin Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Potential colonization of organisms, including Mycobacteria, in Sorin Heater...

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

Class II — Potential Health HazardOngoing