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. 1,002 recalls have been distributed to Kentucky in the last 12 months.
Showing 28781–28800 of 51,386 recalls
Recalled Item: Persona Stemmed Tibial Provisional Size H Left Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial SZ PLT Size H Left Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed Tibial Provisional Size H Right Recalled by Zimmer Biomet,...
The Issue: There is a potential for intermittent cracks in the raw material batch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...
The Issue: The software is not identifying the patient as having atypical hyperplasia,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Hip Application (THA) Product Usage: The Robotic Arm Interactive...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Bridge Occlusion Balloon catheter Recalled by Spectranetics...
The Issue: Possible inability to pass the guidewire through the Bridge device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.