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. 1,029 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,029 in last 12 months

Showing 20921–20940 of 51,386 recalls

DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: del Nido Cardioplegia Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility; bags have potential to leak

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Ingenus Pharmaceuticals Llc

Recalled Item: Leucovorin Calcium Injection Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Crystallization: Presence of particulate matter identified as API...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl Recalled by...

The Issue: Lack of Assurance of Sterility; bags have potential to leak

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas infinity central lab / cobas infinity core license-a Calculator/Data...

The Issue: Cobasinfinity laboratory solution Version 2.4.1 through Version 2.5.4 Using...

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

Class II — Potential Health HazardOngoing
FoodOctober 8, 2019· Blue Bell Creameries, L.P.

Recalled Item: Blue Bell Butter Crunch Ice Cream packaged in a 1/2 Recalled by Blue Bell...

The Issue: Possible foreign material in product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2019· Implant Direct Sybron Manufacturing LLC

Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Some dental implant packages contain incorrect implants, which could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Smith & Nephew, Inc.

Recalled Item: LAG SCREW 3.2MM GUIDE PIN SLEEVE Recalled by Smith & Nephew, Inc. Due to LAG...

The Issue: LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Edwards Lifesciences, LLC

Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...

The Issue: Intermittent communication due to inconsistent crimping of connectors onto...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Beckman Coulter, Inc.

Recalled Item: UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Recalled...

The Issue: When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· The Binding Site Group, Ltd.

Recalled Item: Optilite Optilite Rheumatoid Factor Kit Recalled by The Binding Site Group,...

The Issue: Assigned Rheumatoid Factor (RF) calibrator value for calibrator component...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Nova Ortho-Med Inc

Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...

The Issue: Walkers within the identified serial range have the potential for the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...

The Issue: Software issue identified in the software versions syngo CT VB20 running on...

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2019· Mylan Laboratories Limited (Sterile Products Division)

Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...

The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 4, 2019· KVK-Tech, Inc.

Recalled Item: Methylphenidate Hydrochloride Oral Solution 5mg per 5mL Recalled by...

The Issue: Presence of Foreign Substance; Fiber particles.

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

Class III — Low RiskOngoing
Refund