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. 2,739 recalls have been distributed to Florida in the last 12 months.
Showing 22321–22340 of 55,837 recalls
Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK AutoEndo5 Recalled by Teleflex Medical Due to Certain clip appliers...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...
The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis MAXI LD PTA Dilatation Catheter Recalled by Cordis Corporation Due to...
The Issue: Product was manufactured utilizing an expired inner body.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By:...
The Issue: Product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen blackberries Recalled by G&C Food Distributors, Inc. Due to Product...
The Issue: Product is contaminated with norovirus.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft Recalled by Ethicon...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection Recalled...
The Issue: Lack of Assurance of Sterility: Bag has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Component for Laser Scanning Microscopes (LSM 700 Recalled by Zeiss, Carl...
The Issue: When the user tilts the transmitted light arm of the microscope to the end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4mm x 2.5 Fluted Pin Pouch Recalled by Exactech, Inc. Due to Potential for...
The Issue: Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega...
The Issue: There is a potential for the screws to have become loosened during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.