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. 2,646 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,646 in last 12 months

Showing 57615780 of 28,748 recalls

Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing): 180-Gram Cement Cartridge with...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS XT Chemistry Products ALKP Slides Recalled by Ortho-Clinical...

The Issue: Samples containing high levels of ALKP (or an interfering substance) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides Recalled by Ortho-Clinical...

The Issue: Samples containing high levels of ALKP (or an interfering substance) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Empowr Knee Recalled by Encore Medical, LP Due to Orthopedic...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Delta Ceramic Femoral Head Recalled by Encore Medical, LP Due...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: CLP Hip Recalled by Encore Medical, LP Due to Orthopedic...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Reverse Shoulder System (RSP) Semi Humeral Socket Insert...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Altivate Reverse Recalled by Encore Medical, LP Due to...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: HUDSON RCI Addipak Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Product dispositioned for scrap for sterility failure investigation that was...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 3, 2023· Ansell Healthcare Products LLC

Recalled Item: NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell...

The Issue: Some surgical glove sterile pouches were not completely sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· LivaNova Deutschland GmbH

Recalled Item: 3T Heater Cooler System Recalled by LivaNova Deutschland GmbH Due to The...

The Issue: The firm's labeling (Quick Guide) contains incorrect information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· Ansell Healthcare Products LLC

Recalled Item: GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell Healthcare...

The Issue: Some surgical glove sterile pouches were not completely sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· Accuray Incorporated

Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...

The Issue: It is possible the upper roller bracket in the Radixact System gantry...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2023· Philips Healthcare

Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...

The Issue: Philips has identified three software issues with compliance concerns to...

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

Class II — Potential Health HazardOngoing