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. 989 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
989 in last 12 months

Showing 35101–35120 of 51,386 recalls

Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Liver Access and Biopsy Needle Set Biopsy needle kit Intended Recalled by...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Centimeter Sizing Catheter Beacon Tip White Vessel Sizing...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Haskal Transjugular Intrahepatic Portal Access Set Introducer Recalled by...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Torcon NB Advantage Catheter Catheter Recalled by Cook Inc. Due...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Aprima Access Nonvascular Introducer Set Accessories Recalled by Cook Inc....

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Kumpe Access Catheter Cathether Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
FoodApril 15, 2016· Frank L Harter & Sons Inc

Recalled Item: HAWAIIAN DELIGHT ING: IMITATION SOUR DRESSING Recalled by Frank L Harter &...

The Issue: The firm failed to include the allergens, Milk and Soy, on the label.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 15, 2016· UNFI

Recalled Item: COMMERCIAL WHEAT GERM 274000 Recalled by UNFI Due to Potential E. coli...

The Issue: Product contains generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2016· Frank L Harter & Sons Inc

Recalled Item: PASTA SALAD ING: PASTA Recalled by Frank L Harter & Sons Inc Due to The firm...

The Issue: The firm failed to include the allergens, Milk and Soy, on the label.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 15, 2016· FoodState, Inc

Recalled Item: MegaFood Multi for Women 40+ Recalled by FoodState, Inc Due to Multi Vitamin...

The Issue: Multi Vitamin label fails to have required warning statement for iron and...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2016· Health 4 Life, LLC

Recalled Item: Passion 4 Life 30 FL oz. Bottle Recalled by Health 4 Life, LLC Due to...

The Issue: Undeclared whey protein containing the allergens of milk and soy lecithin.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 15, 2016· Frank L Harter & Sons Inc

Recalled Item: SPINACH DIP ING: VEGETABLE SOUP MIX Recalled by Frank L Harter & Sons Inc...

The Issue: The firm failed to include the allergens, Milk and Soy, on the label.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Merge Healthcare, Inc.

Recalled Item: Merge LIS software. The firm name on the label is Recalled by Merge...

The Issue: There are potential issues with results reporting for certain run-based...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing