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. 2,622 recalls have been distributed to Florida in the last 12 months.
Showing 43701–43720 of 55,837 recalls
Recalled Item: 8 in. chipotle flavored tortilla wraps Recalled by El Popocatepetl Ind.,...
The Issue: El Popocatepetl Ind., Inc. of Chicago, Illinois is voluntarily recalling El...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 8 in. spinach pesto flavored tortilla wraps Recalled by El Popocatepetl...
The Issue: El Popocatepetl Ind., Inc. of Chicago, Illinois is voluntarily recalling El...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Catalys Precision Laser System-Catalys - U - US product Recalled by...
The Issue: Software anomaly on OptiMedica CATALYS System version 3.00.05 that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008T with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 Recalled...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Abbott Medical Optics,...
The Issue: Device may experience loss of suction during treatment resulting in scoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY Recalled by...
The Issue: Failures of the 4.8mm of the GAP Endo-Exo Medullary System have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004 Recalled by TITAN SPINE,...
The Issue: The TCS Straight Hexlobular #6 Drivers (5210-1004) tip sheared off during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...
The Issue: The recalling firm was notified by the contract manufacturer that they had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caviwave Pro Ultrasonic Cleaning System Recalled by Steris Corporation Due...
The Issue: Should the Caviwave Pro Ultrasonic Cleaning System experience a temporary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers Recalled by Steris Corporation Due...
The Issue: STERIS has identified that the control board software in select AMSCO 400...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Q-Syte Luer Access Split Septum Recalled by Becton Dickinson & Company...
The Issue: Becton Dickinson received an elevated number of complaints for blood or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Lack of Assurance of Sterility; due to leaking vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Lack of Assurance of Sterility; due to leaking vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Spirit TM Select bed is a Med-Surg bed intended Recalled by CHG Hospital...
The Issue: It was identified that in some situations the bed exit alarm may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza. A Picture Archiving and Communication System (PACS) intended to...
The Issue: Possibly incomplete archived studies during pre-fetch. In a server farm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velocity" Biopsy Valve Recalled by US Endoscopy Group Inc Due to The company...
The Issue: The company has received reports of structural non conformance at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOS Recalled by Eos Imaging Inc Due to When performing calibration, an alert...
The Issue: When performing calibration, an alert message on the spectral filtration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.