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. 1,005 recalls have been distributed to Florida in the last 12 months.
Showing 38381–38400 of 55,837 recalls
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....
The Issue: The center bolt of the sling bar, which connects the bar to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva Emit Methotrexate Assay Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics confirmed that Syva Emit Methotrexate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments...
The Issue: Reports relating to unintended patient or operator burns or operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...
The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Triglyceride_2 Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics has confirmed the ADVIA Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRIdian ViewRay Radiation Therapy System Recalled by Viewray Incorporated...
The Issue: When editing the isocenter or the couch position of the plan while in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments...
The Issue: Reports relating to unintended patient or operator burns or operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Brilliance Workspace NM Nuclear medicine image display and...
The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management...
The Issue: Complaints were received of restricted/inaccurate flow rate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal DX/HX/EX AutoSPECT Pro Software Application Recalled by...
The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Brilliance Workspace NM Special Nuclear medicine image display and...
The Issue: The AutoSPECT Pro application was only designed to reconstruct cardiac SPECT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spectra-System Dental Implant 2008 system is comprised of dental...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling GoDirect Implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions became aware of a potential problem with the click...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...
The Issue: Materne North America Corp. is voluntarily recalling specific packages of...
Recommended Action: Do not consume. Return to store for a refund or discard.