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.

51,386 total recalls
1,002 in last 12 months

Showing 28721–28740 of 51,386 recalls

DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate (CHG)...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q.Care Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Toothette Oral Care Short Term Oral Swab System with Antiseptic Oral Rinse...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Oral Cleansing & Suctioning System with 0.12% Chlorhexidine Gluconate (CHG)...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Wockhardt Usa Inc.

Recalled Item: Enalapril Maleate tablets Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: 5mg strength being recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Oral Cleansing & Suctioning System q2 with 0.12% Chlorexidine Gluconate...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: QCare RX Q2 Oral Cleansing & Suctioning System with 0.12% Recalled by Sage...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Toothette Oral Care Single Use System With Perox-A-Mint solution. Contains:...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q.Care Oral Cleansing & Suctioning System q8. Contains 1 Covered Recalled by...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Ziptight Ankle Syndesmosis Fixation Device Recalled by Zimmer Biomet, Inc....

The Issue: Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2017· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...

The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Philips Electronics North America Corporation

Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...

The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...

The Issue: Software update to correct several issues that include (1)Potential data...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Olympus Corporation of the Americas

Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...

The Issue: Olympus has received complaints about fragments of adhesive which detached...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...

The Issue: Intermittent communication between the host system and the FlexCardio

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Integra LifeSciences Corp.

Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...

The Issue: A quarantined lot of the devices was released for sale. Devices from this...

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

Class II — Potential Health HazardOngoing
DrugAugust 18, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign tablets/capsules: risperidone Tablets were found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2017· Vital Rx, Inc. dba Atlantic Pharmacy and Compounding

Recalled Item: All Sterile Products within expiry Recalled by Vital Rx, Inc. dba Atlantic...

The Issue: Lack of Assurance of Sterility .

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund