State

Kentucky product recalls

72,907 recalls have nationwide distribution and so reach Kentucky. 7,164 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total: 7,164
Critical: 1,399
Severe: 1,694
Most recent: 2026-09-09

Of the 7,164 recalls naming Kentucky we have scored against our rubric, 1,399 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,694 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,164 recalls whose distribution notice names Kentucky specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1026–1050 of 80071

SevereFDA (Devices)·Z-2602-2026·2026-07-01
Abiomed Impella CP Set with SmartAssist 10th Generation Introducer Kit Recall
Abiomed is recalling Impella CP Set with SmartAssist (10th Generation) containing 14Fr Low Profile Introducer Kits due to potential thrombus (blood clot) formation during prolonged use of the introducer.
Product
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13 and 25 cm Japan. Product Code: 1000542.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2585-2026·2026-07-01
Medline 10mL Polycarbonate Syringes in Medical Procedure Kits Recalled
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and in Barbados.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. AAA DYNJ905651B ARTERIOGRAM TRAY 00-402001S AV SHUNT PACK-LF DYNJ0842516F BASIC IR PACK-LF PHS463660F CATH PROCEDURAL TRAY DYNJ43580C CONGENITAL ADD-ON KIT DYN
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1099-2026·2026-07-01
Spring & Mulberry Lavender Rose Chocolate Recalled for Salmonella
Spring & Mulberry Inc. is recalling Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects multiple batch lots distributed nationwide.
Product
Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2599-2026·2026-07-01
Abiomed Impella CP Introducer Kit recalled for thrombus formation risk
Abiomed is recalling 3 units of the 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP due to potential for blood clot formation during prolonged use.
Product
Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000434. Introducer Product Code: 1000434.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1104-2026·2026-07-01
Spring & Mulberry Sea Salt Date-Sweetened Chocolate recalled for Salmonella
Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.
Product
Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individua
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1103-2026·2026-07-01
Spring & Mulberry Date-Sweetened Chocolate Recalled for Salmonella
Spring & Mulberry Inc. is recalling Pure Dark and Pure Dark Minis date-sweetened chocolate products nationwide due to potential Salmonella contamination. Consumers should not consume the affected products and should discard or return them.
Product
1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a navy blue box, UPC 850055470002, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1123-2026·2026-07-01
Sunflower Seeds Recalled for Undeclared Cashew Allergen
George J Howe Company, Inc. is recalling 25-pound cases of sunflower seeds due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across multiple states.
Product
25# Sunflower Seeds C/S
Category
Food
Distribution
25 states
SevereFDA (Devices)·Z-2583-2026·2026-07-01
Medical Device Surgical Kits with Syringes Recalled for Unapproved Design Changes
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes used in surgical procedures. The manufacturer identified unapproved design changes to the products that were not cleared by the FDA through the 510(k) process.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. BARIATRIC DYNJ905153J DYNJ905153K DYNJ905153L GYNE LAPAROTOMY PACK-LF DYNJ49593A LAPAROSCOPY DYNJ905157G DYNJ905157I DYNJ905157J LAPAROSCOPY PACK DYNJ56930B MAJOR PLUS
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1100-2026·2026-07-01
Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars recalled
Spring & Mulberry Inc. is recalling Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars nationwide due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it.
Product
Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470033, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2453-2026·2026-07-01
Medline Convenience Kits with Lidocaine and Bupivacaine Injections Recalled
Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
Product
Medline Convenience Kits: 1) OPEN HEART CDS, Model Number: CDS840144Q; 2) OPEN HEART, Model Number: CDS840150W; 3) OPEN HEART ADULT, Model Number: CDS840396AA; 4) CABG A CDS, Model Number: CDS982269N; 5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G; 6) OPEN HE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2587-2026·2026-07-01
Medline Convenience Kits with Syringes Recalled for Unapproved Design Changes
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CRANIOTOMY PACK-LF DYNJ0101292F DYNJ0101292G HYBRID PACK DYNJ65925A LAMINECTOMY DYNJ905156L DYNJ905156M DYNJ905156N DYNJ905156O DYNJ905156P MAJOR EXTREMITY DYNJ905
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2455-2026·2026-07-01
Medline Convenience Kits Medical Devices Recalled for Quality Issues
Medline Industries is recalling four models of Convenience Kits containing Lidocaine and Bupivacaine injections due to quality issues identified during an FDA inspection of the supplier.
Product
Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC010890; 2) OPEN HEART A OVERHEAD, Model Number: DYNJ910066; 3) OPEN HEART, Model Number: DYNJ9855016V; 4) OPEN HEART, Model Number: DYNJ9855016X
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V424000·2026-07-01
Honda Recalls 2026 Pilot and Passport for Rear Subframe Bolt Defect
Honda is recalling 2026 Pilot and Passport vehicles because improperly tightened rear subframe bolts may lead to vehicle instability or detachment, increasing crash risk.
Product
HONDA — HONDA PASSPORT, PILOT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-1112-2026·2026-07-01
Zapp's Bayou Blackened Ranch Kettle Chips Recalled for Salmonella
Utz Quality Foods, LLC is recalling 1.5oz bags of Zapp's Bayou Blackened Ranch Kettle Chips due to the potential presence of Salmonella. The product was distributed across 32 states.
Product
1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Food)·H-1113-2026·2026-07-01
Zapp's Brand Bayou Blackened Ranch Potato Chips Recalled for Salmonella
Utz Quality Foods is recalling Zapp's Brand Bayou Blackened Ranch Potato Chips in 2.5oz and 8oz bags due to potential Salmonella contamination. Affected products were distributed across 32 states.
Product
2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chips, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Food)·H-1096-2026·2026-07-01
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate Recalled Due to Salmonella
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate bars are recalled due to potential Salmonella contamination. The product was distributed nationwide.
Product
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail produc
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1105-2026·2026-07-01
Spring & Mulberry Coffee Date-Sweetened Chocolate bars recalled for Salmonella
Spring & Mulberry Inc. is recalling Spring & Mulberry Coffee Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.
Product
Spring & Mulberry Coffee Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light brown box, UPC 850055470224, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1102-2026·2026-07-01
Spring & Mulberry Pecan Date Chocolate Recalled for Salmonella Risk
Spring & Mulberry Inc. is recalling approximately 79,156 individually packaged pecan date date-sweetened chocolate bars nationwide due to potential Salmonella contamination.
Product
Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a yellow box, UPC 850055470040, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indiv
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1117-2026·2026-07-01
Utz Quality Foods Dirty Sour Cream Onion Potato Chips Salmonella Recall
Utz Quality Foods is recalling 2.0 oz bags of Dirty Sour Cream and Onion Potato Chips due to potential Salmonella contamination. The product was distributed across 32 US states.
Product
2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Devices)·Z-2591-2026·2026-07-01
Medline angiography and radiology convenience kits recalled for unapproved design changes
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and to Barbados.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO PACK DYNJ30565C DYNJ32555B ANGIO PACK-LF DYNJ0774765U ANGIO TRAY DYNJ46153A ANGIOGRAM TRAY DYNJ33638K ANGIOGRAPHY DRAPE PK QVH-LF DYNJ35110D ANGIOGRAPHY P
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1115-2026·2026-07-01
Utz Dirty Maui Onion Chips Recalled for Potential Salmonella
Utz Quality Foods is recalling 2.0 oz bags of Dirty Maui Onion Chips due to potential Salmonella contamination. The product was distributed across 32 US states.
Product
2.0 oz Dirty Maui Onion Chip, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Food)·H-1097-2026·2026-07-01
Spring & Mulberry Mixed Berry Date-Sweetened Chocolate recalled for potential Salmonella
Spring & Mulberry Inc. is recalling Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects approximately 66,779 individual bars distributed nationwide.
Product
Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indiv
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2600-2026·2026-07-01
Abiomed Impella CP Introducer Kit Recalled for Thrombus Risk
Abiomed is recalling the 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP due to potential thrombus formation during prolonged use. The recall affects 17 units distributed in the United States and Japan.
Product
Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1116-2026·2026-07-01
Zapp's Big Cheezy Potato Chips recalled due to Salmonella risk
Utz Quality Foods, LLC is recalling 1.5oz and 8.0oz bags of Zapp's Big Cheezy Potato Chips due to potential Salmonella contamination. The recalled product was distributed across 32 states.
Product
1.5oz, 8.0oz , Zapp's Big Cheezy Potato Chips, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Devices)·Z-2593-2026·2026-07-01
Medline convenience kits recalled for unapproved syringe design changes
Medline Industries recalls convenience kits containing 10mL polycarbonate colored syringes because design changes were made outside of FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ABDOMINAL VASCULAR-LF DYNJ905291B DYNJ905291C ARTERIOGRAM DYNJ28082G CVICU HEART BAG DYKM2130A ENDOVASCULAR PACK DYNJ0678934J EP PACK DYNJ23456J GENERAL ENDO PA
Category
Medical Device
Distribution
Distributed nationwide