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. 1,736 recalls have been distributed to Kentucky in the last 12 months.
Showing 43201–43220 of 51,386 recalls
Recalled Item: Apri (desogestrel and ethinyl estradiol tablets USP) Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...
The Issue: Trend in reports of unexpected decrease in beam output in C-series High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...
The Issue: Inadequate iodine and packaging related defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brevibloc Premixed Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Complaints received of discolored solution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...
The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...
The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Color
The Issue: Undeclared color Red #3 .
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Colors
The Issue: Undeclared colors Blue #1, Blue #2 and Red #40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Colors
The Issue: Undeclared colors Blue #1, Red #3 and Yellow #5.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vita Classic Premium Sliced Smoked Atlantic Nova Salmon Recalled by Vita...
The Issue: This voluntary recall is being initiated due to a positive Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...
The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...
The Issue: Failed Dissolution Specifications: Stability results found the product did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.