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. 2,918 recalls have been distributed to Florida in the last 12 months.
Showing 4761–4780 of 30,686 recalls
Recalled Item: DIVA 24 Inch Widescreen LCD Touch Display - Used with Recalled by Philips...
The Issue: If the DIVA touch display generates touch inputs without user interaction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mariner RDX Polyaxial Head Recalled by SEASPINE ORTHOPEDICS CORPORATION Due...
The Issue: Screw heads, of pedicle screw systems, have thin lead-in thread that pose a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Rad Recalled by Bio-Rad Laboratories Due to Due to incorrect...
The Issue: Due to incorrect calibrations and controls, their is a potential of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signia" Small Diameter Curved Tip Intelligent Reload Recalled by Covidien,...
The Issue: Under certain firing conditions, reloads were found to articulate in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload Recalled by...
The Issue: Under certain firing conditions, reloads were found to articulate in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cystatin C Calibrator - In vitro diagnostic (IVD) use in Recalled by Randox...
The Issue: Cystatin C Calibrator Series CVS 2699, is running with a negative bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Boot Assembly Recalled by Baxter Healthcare Corporation Due to Three...
The Issue: Three lots of the Boot Assembly, Traction Device are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM...
The Issue: Automated external defibrillators were shipped in their test configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a Recalled...
The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW QuickFlash Radial Artery Catherization (wire Recalled by ARROW...
The Issue: Teleflex is initiating this voluntary recall for the above-mentioned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a Recalled...
The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assembly Recalled by Think Surgical, Inc. Due to There is a galling effect...
The Issue: There is a galling effect (cold-weld) caused by friction between the array...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preat Nobel Active/Conical-compatible RP Titanium Blank Recalled by Preat...
The Issue: Due to a manufacturing issue, the screw seat location on the abutment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: UNclog Eye Mask Product Name: UNclog Eye Mask Recalled by EYE...
The Issue: Due to a change in the safety clips for the heated eye masks, the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Total T4 Recalled by Beckman Coulter, Inc. Due to Four lots of Access...
The Issue: Four lots of Access Total T4 reagent lots demonstrated imprecision outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microStar Reader Recalled by Landauer Due to Permanent discontinuance of the...
The Issue: Permanent discontinuance of the microSTARii medical dosimetry system....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.