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.
Showing 5581–5600 of 30,686 recalls
Recalled Item: Big Bore RT with software version V4.8.0.10421- Model: 728242 CT Recalled by...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to When preparing...
The Issue: When preparing for CCT Fluoroscopy mode and activating the CCT foot pedal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology with software version V4.8.0.10421...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Affiniti 70 Recalled by Philips Ultrasound, Inc. Due to Their is the...
The Issue: Their is the potential that diagnostic ultrasound systems operating with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200)...
The Issue: Their is the potential that diagnostic ultrasound systems operating with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED-810A Zemits NDPrime Laser products Recalled by Advance-Esthetic LLC Due...
The Issue: Advance-Esthetic LLC failed to comply with the applicable standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Da Vinci Single-Site Wristed Needle Driver Recalled by Intuitive Surgical,...
The Issue: There is the potential for the needle drive to become dislodged and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...
The Issue: If "Clear All" selected medications is selected on patient profile, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...
The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...
The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...
The Issue: Due to products distributed without premarket clearance or approvals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...
The Issue: Due to products distributed without premarket clearance or approvals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DENTEMP ONE STEP .077OZ Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.