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. 2,845 recalls have been distributed to Florida in the last 12 months.
Showing 13761–13780 of 30,686 recalls
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to During a...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE Recalled by Karl Storz Endoscopy...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Recalled by Karl Storz Endoscopy Due to During a complaint...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Drill Sleeve Guides Recalled by Ad-Tech Medical Instrument...
The Issue: The inner diameter of the drill sleeve guide raw material was found to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Control Panel 60-02-15: LivaNova SCP Pump Control Panel. Recalled by...
The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Control Panel 60-02-50: LivaNova SCP Pump Control Panel Recalled by LivaNova...
The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...
The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...
The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...
The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Recalled by LivaNova USA Inc Due to Sentiva generators may reset...
The Issue: Sentiva generators may reset and become disabled within 60 days of enabling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...
The Issue: Reports have been received of the CentriMag Systems experiencing motor and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMOD PORCOAT HA GLENTRAY Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.