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. 1,132 recalls have been distributed to Florida in the last 12 months.
Showing 15761–15780 of 30,686 recalls
Recalled Item: AF 550 x 5ML/H FH DL 30hole SAT C Recalled by Arrow International Inc Due to...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AF 550 x 5ML/HR CPNB Recalled by Arrow International Inc Due to Possible...
The Issue: Possible cracks on the body of the fill port connector, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 125 Deg 12x165mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 130 Deg 10x165mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 130 Deg 11x300mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 9x165mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 Deg 11x300mm Recalled by Zimmer Biomet,...
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 125 Deg 10x165mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Recalled by...
The Issue: Laser engraved label does not match with the item in the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left Deg 9x300mm Recalled by Zimmer Biomet, Inc....
The Issue: The set screw is not able to advance or reverse from the original position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Pruitt F3¿-S Polyurethane Outlying Carotid Shunt Recalled...
The Issue: Pouches from this lot are not sealed compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YXLON Cougar Cabinet X-Ray System Product Usage: The products are Recalled...
The Issue: Failure to meet the requirement of the performance standard for cabinet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YXLON Cheetah cabinet X-Ray System Product Usage: The products are Recalled...
The Issue: Failure to meet the requirement of the performance standard for cabinet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C3 Wave App Recalled by Medical Components, Inc dba MedComp Due to When the...
The Issue: When the iPad is updated with Apple iOS software version 12, the C3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P28 Recalled by Paragon 28, Inc. Due to Mislabeling
The Issue: It has been determined that the wedge implant kit is permanently mislabeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to There is a...
The Issue: There is a possibility that the liquid suction pump on some AIA-2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Horizon a) 3R Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: The terminals on the plug may become loose and overheat.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience has...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Countersink 1.7mm Recalled by TriMed Inc. Due to The epoxy on Apex...
The Issue: The epoxy on Apex manufactured epoxy-coated instruments can pop off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-2000 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...
The Issue: Tosoh Bioscience has become aware of a potential issue with the AIA-900 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.