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. 2,639 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,639 in last 12 months

Showing 66816700 of 51,386 recalls

Medical DeviceFebruary 8, 2024· Baxter Healthcare Corporation

Recalled Item: CLEARLINK Non-DEHP Solution Set Luer Lock Adapter Recalled by Baxter...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
FoodFebruary 7, 2024· Trader Joe's Company

Recalled Item: Trader Joe s Cilantro Salad Dressing (SKU 36420) Perishable Keep Recalled by...

The Issue: L. mono contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 7, 2024· Trader Joe's Company

Recalled Item: Trader Joe s Elote Chopped Salad Kit (SKU 74768) 11.94 oz. Recalled by...

The Issue: L. mono contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 7, 2024· Trader Joe's Company

Recalled Item: Trader Joe s Southwest Salad (SKU 56077) 9 oz. Recalled by Trader Joe's...

The Issue: L. mono contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 7, 2024· Taylor Fresh Foods Inc

Recalled Item: Marketside Bacon Ranch Crunch Chopped Salad Kit 12.76oz Recalled by Taylor...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 7, 2024· Taylor Fresh Foods Inc

Recalled Item: COLD CASE Recalled by Taylor Fresh Foods Inc Due to Potential Listeria...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 7, 2024· Life Technologies Corporation

Recalled Item: Torrent Suite Dx Software versions 5.14 and earlier used in Recalled by Life...

The Issue: Torrent Suite Dx Software versions 5.14 and earlier used in connection with...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Beckman Coulter, Inc.

Recalled Item: Access Substrate Recalled by Beckman Coulter, Inc. Due to On 07 February...

The Issue: On 07 February 2024 Beckman Coulter made the decision to conduct a field...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Natus Neurology Inc

Recalled Item: TENSIVE Conductive Adhesive Gel Recalled by Natus Neurology Inc Due to Natus...

The Issue: Natus has become aware that its third-party supplier Parker Laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Smiths Medical ASD Inc.

Recalled Item: smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP...

The Issue: When a paraPAC plus ventilator is switched to the operating mode of...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2024· Smiths Medical ASD Inc.

Recalled Item: smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP...

The Issue: When a paraPAC plus ventilator is switched to the operating mode of...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2024· Natus Neurology Inc

Recalled Item: natus neurology Recalled by Natus Neurology Inc Due to Natus has become...

The Issue: Natus has become aware that its third-party supplier Parker Laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: DCA Systems HbA1c Reagent Kit Recalled by Siemens Healthcare Diagnostics,...

The Issue: The reason for the recall is that the Siemens DCA HbA1c Reagent Kit was...

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

Class II — Potential Health HazardOngoing
DrugFebruary 6, 2024· Mallinckrodt Hospital Products Inc.

Recalled Item: Acthar Gel (repository corticotropin injection) 400 USP units/5mL (80 USP...

The Issue: cGMP deviations: Temperature excursion due to shipping delay from...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2024· Mallinckrodt Hospital Products Inc.

Recalled Item: Terlivaz (terlipressin for injection) Recalled by Mallinckrodt Hospital...

The Issue: cGMP deviations: Temperature excursion due to shipping delay from...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: Arize Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: SCHWINNNG Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2024· Today The World

Recalled Item: Sustain Herbal Dietary Supplement Recalled by Today The World Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing