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. 2,939 recalls have been distributed to Florida in the last 12 months.
Showing 1801–1820 of 30,686 recalls
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....
The Issue: Incorrect blister labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...
The Issue: It was determined that the consumable issue may result in No Call - INT CTL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....
The Issue: software issue that causes an error screen on a portable vital signs monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number:...
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376....
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient Monitor software update to address issues:1)May freeze at startup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " Recalled by Prismatik...
The Issue: Due to packaging mix up. Package of finished devices were reported to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges...
The Issue: Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus Initial Drill Recalled by Straumann USA LLC Due to The batch was...
The Issue: The batch was produced without the laser engraving of 7 mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Augmedics Perc Pin Adaptor Recalled by Augmedics Ltd. Due to The perc pin...
The Issue: The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microtek Patient Drape ECOLAB AP6MMN Patient Drape Recalled by Microtek...
The Issue: Due to non-sterile products being labeled as sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Recalled by Medical...
The Issue: Potential for DC Power Supply housing to become hot to the touch and deform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Occlusion Catheter. Catalog Numbers: 2103-36 Recalled by LeMaitre...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X)...
The Issue: Potential for the presence of visible foreign matter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09 Recalled by...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.