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. 2,639 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,639 in last 12 months

Showing 65616580 of 28,748 recalls

Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460 Recalled...

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· LumiraDx

Recalled Item: SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample...

The Issue: Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Linkbio Corp.

Recalled Item: LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp....

The Issue: Contains the incorrect implant in the packaging. The packaging incorrectly...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Cepheid

Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...

The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Cepheid

Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...

The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: AVNS ambIT System - PIB/PCA W 2.5in Cath Recalled by Avanos Medical, Inc....

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Abbott Ireland Limited

Recalled Item: Alinity i Anti-TPO Reagent Kit Recalled by Abbott Ireland Limited Due to Due...

The Issue: Due to a manufacturing fill volume error, Alinity i Anti-TPO Reagent...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: SMMT ambIT Kit Basic Filter Luer Cass Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: ambIT Cassette Filter Male Luer Recalled by Avanos Medical, Inc. Due to Some...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: SMMT ambIT Reusable Program - Luer Cass Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2023· Avanos Medical, Inc.

Recalled Item: AVNS ambIT System - PIB/PCA W 5in Cath Recalled by Avanos Medical, Inc. Due...

The Issue: Some of the ambIT kits were potentially distributed without an air in-line...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Drainage Catheter Insertion Tray 15.5F Recalled by Merit Medical...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Pleural Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2023· Merit Medical Systems, Inc.

Recalled Item: Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F Recalled by Merit...

The Issue: There is a potential that valve assemblies will not open. preventing fluid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing