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. 1,726 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,726 in last 12 months

Showing 4808148100 of 51,386 recalls

Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Custom Spine, Inc.

Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...

The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro/ Sure-Pro Ultra Embryo Replacement Catheters (with...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro¿ Single Stage Embryo Replacement Catheter Product Code:...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner and Reprocessor System Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter with Obturator...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N8371: Non-DEHP Y-Type Catheter Extension Set Kit Recalled...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Stylet Product...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Corp. AxSOS System Instrument. The AxSOS Locking...

The Issue: Stryker Orthopaedics has received a report indicating that the scale of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Transonic Systems Inc

Recalled Item: HCS3011 AV Loop Kit For use with Transonic CO status System Only Recalled by...

The Issue: Transonic Systems Inc. have received complaints of blood leakage involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Abbott Molecular

Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...

The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...

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

Class III — Low RiskOngoing
Medical DeviceMarch 28, 2013· Elekta, Inc.

Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...

The Issue: The problem is that the "static tolerances" from the calibration files...

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

Class II — Potential Health HazardOngoing
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Mocha Recalled by NuGo Nutrition HQ Due to Undeclared Milk

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Pretzel 1.59 oz (45g) Non-Dairy Non-Dairy Recalled by NuGo...

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Free Carrot Cake Recalled by NuGo Nutrition HQ Due to Undeclared Milk

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Peanut Butter Cup Recalled by NuGo Nutrition HQ Due to Undeclared Milk

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Mint Chocolate Chip Recalled by NuGo Nutrition HQ Due to...

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Dark Chocolate Chocolate Chip 1.59 oz (45g) Non-Dairy Recalled by NuGo...

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Slim Espresso Recalled by NuGo Nutrition HQ Due to Undeclared Milk

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2013· NuGo Nutrition HQ

Recalled Item: NuGo Free Dark Chocolate Crunch Recalled by NuGo Nutrition HQ Due to...

The Issue: Product may contain undeclared milk product

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

Class I — Serious Health HazardOngoing
Refund