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. 2,824 recalls have been distributed to Florida in the last 12 months.
Showing 17121–17140 of 55,837 recalls
Recalled Item: Bueno Coffee Substitute Pecan Praline Recalled by Creative Foods Inc Due to...
The Issue: Bueno Coffee Substitute Pecan Praline Gluten-Free product contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Estradiol Transdermal System Delivers 0.0375 mg/day Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for release rate testing and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Delivers 0.075 mg/day Recalled by...
The Issue: Defective Delivery System: Out of specification for release rate testing and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxygen Recalled by Grace Healthcare Medical, Inc Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colpassist Vaginal Positioning Device - Product Usage: intended for use...
The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UpsylonTM Y Mesh Kit with Colpassist Vaginal Positioning Device - Recalled...
The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits Recalled...
The Issue: Cannulated Screwdrivers may break at the driver tip along the shaft, near...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change...
The Issue: Compromised sterile barriers due to the Tyvek Lid not properly adhering to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eyesuite 9.3.1 software Recalled by Haag-Streit USA Inc Due to Examination...
The Issue: Examination data and patient name may be mixed up when printing or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illuminated Stepped Laser Probe Curved-for use in combination with 23G...
The Issue: Barcode label extended expiration date. Barcode located at the short side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer ABL90 FLEX PLUS Analyzer with E3800 PC units. The Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E3800 PC Units (spare parts) Recalled by Radiometer Medical ApS Due to Due...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to specimens...
The Issue: specimens collected in transport media may result is false negative results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delflex Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...
The Issue: Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dry Eye Test Recalled by Nomax Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended...
The Issue: Cooling Unit (CLU) expelled out of a CT gantry of an iCT system may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 15 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI RDS VENOUS STENT System Product Usage: is indicated for Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI VENOUS STENT System Product Usage: is intended for the Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.