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. 1,002 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,002 in last 12 months

Showing 28901–28920 of 51,386 recalls

FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Major D-Vita Drops Recalled by The Harvard Drug Group Due to The...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· Amrita Health Foods

Recalled Item: Amrita Chocolate Chip Coconut 15g Protein Bar Recalled by Amrita Health...

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
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Ferrous Sulfate Liquid One Pint Recalled by The Harvard Drug Group Due...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· Amrita Health Foods

Recalled Item: Amrita Pineapple Chia Energy Bar Recalled by Amrita Health Foods Due to...

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
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Liquid Vitamin C Supplement Recalled by The Harvard Drug Group Due to...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Leader Liquid Multivitamin Supplement for Infants and Toddlers Recalled by...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Polyvitamin Liquid with Iron Recalled by The Harvard Drug Group Due to...

The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2017· Zimmer Biomet, Inc.

Recalled Item: Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled Recalled by...

The Issue: The products being recalled exceeded the weight previously tested leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Segmental System Recalled by Zimmer Biomet, Inc. Due to The products...

The Issue: The products being recalled exceeded the weight previously tested leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2017· Cardinal Health 200, LLC

Recalled Item: Presource(R) Kits (custom surgical/procedural kits): The standard and custom...

The Issue: The firm manufactured and distributed Presource(R) kits which contained BD...

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2017· The Ampt Life, LLC

Recalled Item: NATURAL HERBAL COFFEE AMPT Recalled by The Ampt Life, LLC Due to Undeclared...

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

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 185 cm (73") Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 85" (216 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 80" (203 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 84" (213 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 137" (348 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· Cook Inc.

Recalled Item: Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane...

The Issue: Central venous catheters may not fit over guide wire potentially causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 139" (353 cm) Y-Type Blood Set w/ 170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 125" (318 cm) Bifuse Blood Set w/170 Micron Filter Recalled by ICU Medical,...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2017· ICU Medical, Inc.

Recalled Item: 98" (249 cm) Y-Type Admin Set w/170 Micron Blood Filter Recalled by ICU...

The Issue: Some devices were labeled as Does not contain DEHP even though the product...

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

Class II — Potential Health HazardOngoing