Product Recalls in Kentucky
Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,027 recalls have been distributed to Kentucky in the last 12 months.
Showing 24601–24620 of 51,386 recalls
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: 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: Affixus Hip Fracture Nail 130 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: AF w/AS 550 x 1-14ML/HR CPNB 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 w/AS 550 x 1-14 ml/hr 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: AF 550 x 5ML/H 6" CATH 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: 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: TriMed Hex Driver 1.2 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: TriMed Locking Drill Guide 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: TriMed Wrist Hook Dorsal Impactor Recalled by TriMed Inc. Due to The WHD/WHV...
The Issue: The WHD/WHV impactors can rust over time due to an improper manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Peg Guide Extender Recalled by TriMed Inc. Due to The spring on the...
The Issue: The spring on the PEG-Extender can rust due to the type of steel used to...
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: 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: 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: Dimension Thermal Chamber Motor Cable located in the following models:...
The Issue: Thermal chamber motors have electrical cables with single insulation rather...
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.