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. 2,601 recalls have been distributed to Kentucky in the last 12 months.
Showing 13501–13520 of 28,748 recalls
Recalled Item: MiniMed Insulin Pump Recalled by Medtronic MiniMed Due to The action is...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Veo Insulin pump Recalled by Medtronic MiniMed...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed Paradigm 512 Insulin pump Recalled by Medtronic MiniMed Due to The...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to The...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed Paradigm Model 511 Insulin Pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Veo Insulin pump Recalled by Medtronic MiniMed...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...
The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...
The Issue: EXACTAMED 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 10 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Cuvette Segments for BN ProSpec System-IVD a system for Recalled by...
The Issue: Iincreased (falsely elevated) Albumin results compared to expected results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Recalled by Agfa...
The Issue: The exposed area of fluo exams possibly does not match the active area of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x120 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 2.5x150mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x34 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x95 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.