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. 1,806 recalls have been distributed to Kentucky in the last 12 months.
Showing 35901–35920 of 51,386 recalls
Recalled Item: Trinity Acetabular Shell Product Usage Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Acetabular System Product Usage - Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Acetabular Shell Product Usage: Total Hip Replacement. Recalled by...
The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crosslock DVR ePAK -Sterile Recalled by Biomet, Inc. Due to Foreign Object...
The Issue: Components of the DVR ePAKs can oxidize during shipment and storage prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video...
The Issue: The firm has become aware of the potential for disruption (flickering) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PINPOINT Endoscopic Fluorescence Imaging System Recalled by Novadaq...
The Issue: It has been determined that the PINPOINT Operator's Manual does not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: software for Syngo Dynamics a Picture Archiving and Communication System...
The Issue: Siemens is releasing a software update that addresses an issue of mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurities/Degradation Specifications: out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Large Volume Paracentesis Kit is packaged in a thermaformed tray Recalled by...
The Issue: Customers have reported that the pinch clamp on the RP Bag was missing....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conformis iTotal Cruciate Retaining (CR) Knee Replacement System Model:...
The Issue: Incorrect femoral component distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atorvastatin Calcium 40 mg Recalled by Golden State Medical Supply Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium 10 mg Recalled by Golden State Medical Supply Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium 20 mg Recalled by Golden State Medical Supply Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium 80 mg Recalled by Golden State Medical Supply Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Menthocin Patch with Lidocaine-Strong (Menthol 5% Recalled by Bonita...
The Issue: Marketed without an approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Figi's Classic Marzipan Recalled by Figi's, Inc Due to Figi's Companies is...
The Issue: Figi's Companies is recalling 8 ounce packages of "Classic Marzipan" because...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Purple Cow Limited Edition Cookie Butter Ice Cream Recalled by House Of...
The Issue: House of Flavors, Inc. is voluntarily recalling a small batch of 8 oz. cups...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature...
The Issue: The firm became aware that when using EtC02 in the kPa or % setting and in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...
The Issue: Failed Dissolution Specification: Out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...
The Issue: Failed Dissolution Specification: Out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.