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. 2,815 recalls have been distributed to Florida in the last 12 months.
Showing 17061–17080 of 30,686 recalls
Recalled Item: Hobbs Bronchial Cytology Brushes Recalled by Hobbs Medical, Inc. Due to...
The Issue: Device was marketed for uses outside the 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATHFAST Myoglobin II reagent cartridge Catalog Number: PF1111-K PATHFAST¿...
The Issue: A pinhole caused by the laser printer in the aluminum sheet over the ALP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATHFAST NTproBNP Catalog Number: PF1061-KUS PATHFAST¿ NTproBNP is a product...
The Issue: A pinhole caused by the laser printer in the aluminum sheet over the ALP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.