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. 2,899 recalls have been distributed to Florida in the last 12 months.
Showing 8841–8860 of 55,837 recalls
Recalled Item: GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell Healthcare...
The Issue: Some surgical glove sterile pouches were not completely sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...
The Issue: It is possible the upper roller bracket in the Radixact System gantry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rasagiline Tablets 0.5mg Recalled by Aurobindo Pharma USA Inc. Due to Failed...
The Issue: Failed dissolution specifications - results obtained were below spec average.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Pain Relieving Cream (Menthol 7.4%) Recalled by Parker Laboratories,...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Tri-Active Therapy Cream (Camphor 3.2% Recalled by Parker...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix CBD Therapy Cream (Menthol 7.4%) Recalled by Parker Laboratories, Inc....
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix CBD Clinical Cream (Menthol 7.4%) Recalled by Parker Laboratories,...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%) Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...
The Issue: Philips has identified three software issues with compliance concerns to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IO Inspired Organics brand Organic Raw Walnut Halves & Pieces Recalled by...
The Issue: undeclared walnuts in ingredient and contains statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SynCardia 50cc TAH-t Recalled by SynCardia Systems LLC Due to Artificial...
The Issue: Artificial hearts contain a epoxy resin that has not been reviewed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70H Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix¿ / Epidural anesthesia set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Product may be mislabeled with an incorrect lid stock label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The incorrect product labeling was applied to the product indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users reported "System Over Temperature" alarms associated with a loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.