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. 2,630 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,630 in last 12 months

Showing 94019420 of 51,386 recalls

Medical DeviceMay 8, 2023· Galt Medical Corporation

Recalled Item: Tearaway Introducer Set Recalled by Galt Medical Corporation Due to Sheath...

The Issue: Sheath introducer assemblies could potentially, due to improper storage...

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

Class II — Potential Health HazardOngoing
FoodMay 6, 2023· Meijer Inc

Recalled Item: Meijer Sweet & Salty Trail Mix 12oz. pouch Recalled by Meijer Inc Due to...

The Issue: Contains undeclared ingredients including wheat and sesame

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 5, 2023· Vyaire Medical

Recalled Item: bellavista 1000e Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...

The Issue: Vyaire Medical identified two patient safety risks during the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2023· Vyaire Medical

Recalled Item: bellavista 1000 Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...

The Issue: Vyaire Medical identified two patient safety risks during the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: Betta Link LG Reusable Fishmouth Guide-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in Recalled by T.A.G....

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: Betta Link LG Reusable ProngED Guide - Intended for use Recalled by T.A.G....

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165 CM 10/BX- Intended Recalled...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165CM 5/BX- Intended for...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230 CM 10/BX- Intended Recalled...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230CM 5/BX- Intended for...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
DrugMay 3, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Buprenorphine Sublingual Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2023· Denison Pharmaceuticals, LLC

Recalled Item: Pin-Away PYRENTAL PAMOATE (Pyrantel base 50 mg / mL) Pinworm Treatment...

The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2023· Denison Pharmaceuticals, LLC

Recalled Item: Safe tussin PM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...

The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2023· Denison Pharmaceuticals, LLC

Recalled Item: Colic Calm Recalled by Denison Pharmaceuticals, LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2023· Denison Pharmaceuticals, LLC

Recalled Item: Safe tussin DM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...

The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 3, 2023· Avery Brewing Company

Recalled Item: Gose con Sandia Recalled by Avery Brewing Company Due to Due to over...

The Issue: Due to over pressurization, can may fail/explode.

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

Class II — Potential Health HazardOngoing
Refund