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. 2,672 recalls have been distributed to Kentucky in the last 12 months.
Showing 1741–1760 of 28,748 recalls
Recalled Item: 3M Ranger Irrigation Fluid Warming Set Recalled by 3M Company Due to Notice...
The Issue: Notice was issued to clarify flow rates related to the inlet fluid temperature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Solos Recalled by ICU Medical, Inc. Due to Internal testing...
The Issue: Internal testing found that Plum Duo pumps with software version 1.1.1 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Duo Recalled by ICU Medical, Inc. Due to Internal testing...
The Issue: Internal testing found that Plum Duo pumps with software version 1.1.1 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI...
The Issue: Affected kits contain recalled Integra Lifesciences Codman Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY...
The Issue: Affected kits contain recalled Integra Lifesciences Codman Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI...
The Issue: Affected kits contain recalled Integra Lifesciences Codman Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Catalyst+ Product Name: C4D software used in conjunction...
The Issue: Software issue with scanning equipment that can results in the filed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm...
The Issue: Firm has received an increase in reports regarding inadvertent instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Sampling Set Recalled by Capnia Inc Due to Sampling set nasal...
The Issue: Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOWER EXTREMITY Recalled by American Contract Systems, Inc. Due to Test...
The Issue: Test results for cast padding component included in procedure trays shows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN...
The Issue: Due to a manufacturing defect IV catheter may have a hole in the septum,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Single Intragastric Linton Balloon Tube Recalled by C.R. Bard Inc Due...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....
The Issue: Incorrect blister labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...
The Issue: It was determined that the consumable issue may result in No Call - INT CTL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.