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 34201–34220 of 51,386 recalls

Medical DeviceJune 2, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Total T4 Reagent Pack Recalled by...

The Issue: Ortho-Clinical Diagnostics confirmed that sample results generated from...

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

Class II — Potential Health HazardOngoing
FoodJune 2, 2016· The Quaker Oats Company

Recalled Item: Quaker Quinoa Granola Bars Recalled by The Quaker Oats Company Due to...

The Issue: SunOpta expanded their recall of listeria Monocytogenes in sunflower...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· Ach Food Companies Inc

Recalled Item: Salad topping labeled under the following brand names: (Product 1) Recalled...

The Issue: Product manufactured with ingredient which may be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· Atlantic Spice Co., Inc.

Recalled Item: Atlantic Spice Cranberry Health Mix Recalled by Atlantic Spice Co., Inc. Due...

The Issue: Product was processed on the same equipment as product possibly contaminated...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· The Quaker Oats Company

Recalled Item: Quaker quinoa granola bars Recalled by The Quaker Oats Company Due to...

The Issue: SunOpta expanded their recall of listeria Monocytogenes in sunflower...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· Atlantic Spice Co., Inc.

Recalled Item: Atlantic Spice Sunflower Seeds Roasted Salted Recalled by Atlantic Spice...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 2, 2016· Atlantic Spice Co., Inc.

Recalled Item: Atlantic Spice Tropical Mix Recalled by Atlantic Spice Co., Inc. Due to...

The Issue: Product was processed on the same equipment as product possibly contaminated...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 1, 2016· Becton Dickinson & Co.

Recalled Item: PhoenixSpec Calibrator & Kit is used to calibrate the PhoenixSpec Recalled...

The Issue: BD has determined that the BBL PhoenixSpec Calibrator kits in this recall...

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

Class III — Low RiskOngoing
Medical DeviceJune 1, 2016· Becton Dickinson & Co.

Recalled Item: PhoenixSpec AP Calibrator is used to calibrate the PhoenixSpec &#38 Recalled...

The Issue: BD has determined that the PhoenixSpec AP Calibrator in this recall from the...

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

Class III — Low RiskOngoing
DrugJune 1, 2016· Aidarex Pharmaceuticals LLC

Recalled Item: Ciprofloxacin OPTH 0.3% SOL Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMay 31, 2016· Teva North America

Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva North America Due...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.946 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.250 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Pentax Video Bronchoscope Designed to be used with a Pentax Recalled by...

The Issue: Pentax America Inc. is recalling various bronchoscopes which contain an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Hologic, Inc

Recalled Item: ATEC CANISTER. Suction Canister with Lid 490 cc. Recalled by Hologic, Inc...

The Issue: Cracks ATEC Canister Lids.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.221 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Ultrasound Video Bronchoscope The EB-1970UK Recalled by Pentax of America...

The Issue: The EB-1970UK Ultrasound Video Bronchoscope shipped between the clearance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.231 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.211 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.012 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing