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. 1,897 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,897 in last 12 months

Showing 1822118240 of 51,386 recalls

DrugJuly 30, 2020· Albek De Mexico S.A. De C.V.

Recalled Item: Assured Instant Hand Sanitizer Vitamin E and Aloe (Ethyl Alcohol 70% v/v)...

The Issue: CGMP Deviations: Next Advanced Antibacterial Hand Sanitizer was found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2020· Ecolab Inc

Recalled Item: Hand Sanitizer (Alcohol 80% v/v) topical solution Recalled by Ecolab Inc Due...

The Issue: Discoloration and Presence of Foreign Substance

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 30, 2020· Thera Test Laboratories, Inc.

Recalled Item: EL-Anti-SARS-CoV-2 IgM Kit Recalled by Thera Test Laboratories, Inc. Due to...

The Issue: Device did not meet the updated EUA packet requirements for positive percent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· Cardinal Health 200, LLC

Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...

The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 10 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 2 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Subpotent Drug:...

The Issue: Subpotent Drug: Out-of-Specification potency results at the 30-day stability...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 29, 2020· SUN VALLEY FOODS LLC

Recalled Item: Material Number 7002 Unique Tracking Number 1000035843 3/8" Diced Green...

The Issue: Potential to contain foreign material

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Vanilla Non-Dairy Frozen Dessert in pint sized Recalled by...

The Issue: Undeclared cashews in the product.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Chocolate Non-Dairy Frozen Dessert in pint sized Recalled...

The Issue: Undeclared cashews in the product.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint Recalled by...

The Issue: Undeclared cashews in the product.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing