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 18841–18860 of 55,837 recalls

Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Ra Medical Systems, Inc.

Recalled Item: DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in Recalled by Ra...

The Issue: Due to footswitch not meeting required specification for protection from...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Zyphr Disposable Cranial Perforator Recalled by Stryker Instruments...

The Issue: Potential for the inner bit to contain a crack, that may or may not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2020· Angiodynamics, Inc.

Recalled Item: Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous...

The Issue: 5F Micro-Introducer Kits may not contain the correct device, packaged with a...

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

Class II — Potential Health HazardOngoing
FoodOctober 14, 2020· Hadson (Toko) Trading Co., Inc.

Recalled Item: Eishindo brand "CUP JELLY (MINI) Recalled by Hadson (Toko) Trading Co., Inc....

The Issue: Product is a choking hazard.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 13, 2020· Luminex Corporation

Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...

The Issue: Luminex has determined that three (3) separate test fixtures used by field...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2020· Luminex Corporation

Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...

The Issue: Luminex has determined that three (3) separate test fixtures used by field...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· ROi CPS LLC

Recalled Item: Regard - Product Usage: Obstetric Gynecologic specialized manual instrument....

The Issue: Labeling error, incorrect expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
FoodOctober 12, 2020· Nurture Inc. dba Happy Family

Recalled Item: Happy Kid Gluten Free Fruit & Oat Bar Organic Blueberry Recalled by Nurture...

The Issue: Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 12, 2020· Nurture Inc. dba Happy Family

Recalled Item: Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Recalled by...

The Issue: Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and...

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

Class II — Potential Health HazardOngoing
Refund