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. 2,615 recalls have been distributed to Florida in the last 12 months.
Showing 48421–48440 of 55,837 recalls
Recalled Item: Heparin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Subpotent; 18 month time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Malibu Polyaxial Screwdriver Recalled by Integra LifeSciences Corp. Due to...
The Issue: Integra LifeSciences has identified through an investigation of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Needleless Connector Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Needlefree Connector, model number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...
The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109 Recalled by...
The Issue: Dako has initiated a recall of HER2 CISH pharmDxTM Kit because weak red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dried Tapioca Pearl Recalled by New Japan International, Inc. Due to...
The Issue: Product contains unapproved colors, 16185-Amaranth (E123)-Delisted FD&C Red...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Recalled by Horiba...
The Issue: HORIBA Medical is informing all ABX PENTRA MultiCal, N Control, and P...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D and Proteus XR/a equipped with Wireless...
The Issue: GE Healthcare has recently become aware of a software issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crimper Model 9100CR26 The Crimper is indicated for use in Recalled by...
The Issue: Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDITECH Microbiology - Calculator/data processing module Recalled by...
The Issue: Potential for patient results being removed from LAB/EMR.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...
The Issue: Presence of Foreign Tablets: A product complaint was received by a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROHTO Cooling Eye Drops Recalled by The Mentholatum Co. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROHTO Dry Eye Recalled by The Mentholatum Co. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DeRoyal ST. Circumcision Clamp Recalled by DeRoyal Industries Inc Due to...
The Issue: Three lots of circumcision clamps were manufactured out of specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trifurcated Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets USP Recalled by Watson...
The Issue: Failed Tablet/Capsule Specifications; Product contains broken tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products 25-OH Vitamin D Total Calibrators Recalled...
The Issue: Ortho Clinical Diagnostics has determined that the VITROS Immunodiagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.