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.

51,386 total recalls
1,806 in last 12 months

Showing 3538135400 of 51,386 recalls

Medical DeviceMarch 31, 2016· Hologic, Inc

Recalled Item: Hologic InPlex CF Molecular Test (IVD) Recalled by Hologic, Inc Due to...

The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Shimadzu Medical Systems

Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...

The Issue: Report of unintentional movement of table to reverse tilting.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Biocare Medical, LLC

Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...

The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...

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

Class III — Low RiskOngoing
DrugMarch 30, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ondansetron Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; 12 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2016· Alimentos Congelados, S.A. (Pinula)

Recalled Item: Wylwood Fresh Frozen Broccoli Cuts Recalled by Alimentos Congelados, S.A....

The Issue: Alimentos Congelados, S.A. (Pinula) is voluntarily recalling 1,800 cases of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm identified an issue in sample processing when using EZee-Nest...

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

Class III — Low RiskOngoing
Medical DeviceMarch 30, 2016· Teleflex Medical

Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...

The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...

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

Class II — Potential Health HazardOngoing
FoodMarch 29, 2016· Lee Seed Co Inc

Recalled Item: Yogurt Super Soynuts packaged in 16 oz. plastic bags and Recalled by Lee...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2016· R.W. Bakers Co. Inc.

Recalled Item: Meijer Plain Knot Rolls Recalled by R.W. Bakers Co. Inc. Due to Undeclared...

The Issue: R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2016· R.W. Bakers Co. Inc.

Recalled Item: Assorted Dinner Rolls Recalled by R.W. Bakers Co. Inc. Due to Undeclared Peanuts

The Issue: R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU) when used with Merge Recalled by...

The Issue: Eye Station images were not importing properly and were imported under...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....

The Issue: There is a potential connection issue when powering up the Merge Hemo Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...

The Issue: If a reader selects Multi-study review prior to the original study...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: If images are sent without an order in the system, they will be matched with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: Cut lines on the image may present horizontally rather than vertically.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...

The Issue: The software did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· The Anspach Effort, Inc.

Recalled Item: ANSPACH Recalled by The Anspach Effort, Inc. Due to Certain lots of the...

The Issue: Certain lots of the Otologic Curved Micro (OCM) Diamond Ball Burrs may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· The Anspach Effort, Inc.

Recalled Item: ANSPACH Recalled by The Anspach Effort, Inc. Due to Certain lots of the...

The Issue: Certain lots of the Otologic Curved Micro (OCM) Diamond Ball Burrs may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Stryker Endoscopy

Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...

The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Becton Dickinson & Co.

Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...

The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...

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

Class II — Potential Health HazardOngoing