State

Kentucky product recalls

72,933 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 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2726–2750 of 80097

HighFDA (Devices)·Z-1634-2026·2026-04-01
TECNIS Eyhance intraocular lens haptic may stick to the optic
AMO Puerto Rico Manufacturing is recalling TECNIS Eyhance IOLs with the TECNIS Simplicity Delivery System because a limited quantity may have a haptic that sticks to the optic, preventing consistent unfolding.
Product
Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Model/Catalog Number: DIB00 Software Version: N/A Product Description: The TECNIS SIMPLICITY" Delivery System is designed to provide
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0615-2026·2026-04-01
Savannah Bee Company Honey BBQ Sauce Mustard Undeclared Allergens
Savannah Bee Company is recalling Honey BBQ Sauce Mustard bottles containing an undeclared different flavor product with soy and wheat allergens not listed on the label.
Product
SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED VINEGAR, WATER, MUSTARD SEED, SALT, SPICES (INCLUDING PAPRIKA AND TUMERIC), NATURAL FLAVOR, GARLIC), HONEY, WATER, DISTILLED VINEGAR, SUGAR, TOMATO CONCENTRATE, HA
Category
Food
Distribution
45 states
HighFDA (Food)·H-0592-2026·2026-04-01
Trader Joe's Vegetable Fried Rice recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Trader Joe's Vegetable Fried Rice (1 lb bags, Item 5650233) due to glass fragments (1–3 cm long, 2–4 mm wide) found in the product. The recall affects approximately 9.9 million pounds distributed across 40 US states.
Product
Item 5650233 Trader Joe's Vegetable Fried Rice, net wt. 1lb per bag. Retail bag UPC 00521482. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per case. Case UPC 10052148200001. All products are intended t
Category
Food
Distribution
43 states
HighFDA (Devices)·Z-1640-2026·2026-04-01
Olympus PK cutting forceps jaws may break from defective welds
Olympus is recalling PK Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation dur
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1635-2026·2026-04-01
Medtronic MiniMed 780G software defects may cause insulin delivery inaccuracies
Medtronic is recalling MiniMed 780G insulin pumps on software 6.60 and 6.61 because three software defects could result in hypoglycemia or hyperglycemia through inaccurate insulin delivery.
Product
MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1629-2026·2026-04-01
Orthalign drill plate sizes 1-5 may allow excessive bone cut
Orthalign is recalling one lot of the Trimax Pegged Drill Plate sizes 1-5 for the Lantern Knee System because plates manufactured out of specification can result in a bone cut in excess of 0.0800 inches.
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2026·2026-04-01
BiDop 3 pocket Doppler labeling includes uncleared fetal indication
Koven Technology is recalling the BiDop 3 Pocket Doppler packaged with a fetal probe because the product labeling includes a fetal indication for use that is not cleared under its 510(k).
Product
Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0401-2026·2026-04-01
Sodium iodide capsule packs recalled after failing capsule specifications
Radnostix is recalling three lots of the Gelatin Capsule Pack used with the Sodium Iodide I-131 Kit because the product failed tablet and capsule specifications.
Product
SODIUM IODIDE I-131 — SODIUM IODIDE I-131 (SODIUM IODIDE I-131)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1652-2026·2026-04-01
Embrace standard drill tower surgical technique lists mixed-up article numbers
Waldemar Link is recalling the Embrace Drill Tower, Standard/Lateral, because the surgical technique document has mixed-up article numbers in the instrument overview, although the surgical steps are correct.
Product
Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63;
Category
Medical Device
Distribution
15 states
ModerateFDA (Devices)·Z-1651-2026·2026-04-01
Embrace shoulder drill tower surgical technique lists mixed-up article numbers
Waldemar Link is recalling the Embrace Drill Tower because the surgical technique document has mixed-up article numbers in the instrument overview, although the individual surgical steps are correct.
Product
Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;
Category
Medical Device
Distribution
15 states
ModerateFDA (Devices)·Z-1645-2026·2026-04-01
BD Alaris system labeling omits required TLS version for secure Wi-Fi
CareFusion is recalling the BD Alaris System with Guardrails Suite MX because the product labeling does not indicate which TLS version must be enabled on the hospital network for secure Wi-Fi communication.
Product
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1620-2026·2026-04-01
Philips L12-5 ultrasound transducer labelling updated to define useful life
Philips is recalling the L12-5 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L12-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1626-2026·2026-04-01
Philips S5-2 ultrasound transducer labelling updated to define useful life
Philips is recalling one S5-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S5-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1621-2026·2026-04-01
Philips L17-5 ultrasound transducer labelling updated to define useful life
Philips is recalling two L17-5 Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips L17-5 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1625-2026·2026-04-01
Philips S4-1 ultrasound transducer labelling updated to define useful life
Philips is recalling the S4-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips S4-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1628-2026·2026-04-01
Philips X7-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the X7-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips X7-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1624-2026·2026-04-01
Philips OMNI III TEE transducer labelling updated to define useful life
Philips is recalling the OMNI III TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips OMNI III TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1619-2026·2026-04-01
Philips C9-4 ultrasound transducer labelling updated to define useful life
Philips is recalling one C9-4 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips C9-4 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1623-2026·2026-04-01
Philips OMNI II TEE transducer labelling updated to define useful life
Philips is recalling two OMNI II TEE Ultrasound Transducers to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips OMNI II TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1618-2026·2026-04-01
Philips 3D6-2 ultrasound transducer labelling updated to define useful life
Philips is recalling the 3D6-2 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips 3D6-2 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1627-2026·2026-04-01
Philips X3-1 ultrasound transducer labelling updated to define useful life
Philips is recalling the X3-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips X3-1 Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1622-2026·2026-04-01
Philips Mini Multi TEE transducer labelling updated to define useful life
Philips is recalling the Mini Multi TEE Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.
Product
Philips Mini Multi TEE Ultrasound Transducer
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V201000·2026-03-31
2025–2026 Ford Bronco Sport and Maverick Occupant Sensor Recall
Ford is recalling certain 2025–2026 Bronco Sport and Maverick vehicles because the front passenger occupant classification sensor may fail to detect a passenger, risking failure of the airbag to deploy in a crash.
Product
FORD — FORD MAVERICK, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V205000·2026-03-31
2026 Ford Explorer and Mustang Engine Piston Circlip Defect Recall
Ford is recalling certain 2026 Explorer and Mustang vehicles because engine piston circlips may have been incorrectly installed, risking loss of drive power and increasing crash risk.
Product
FORD — FORD EXPLORER, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V202000·2026-03-31
Ford Recalls 2026 Explorer and Aviator for HVAC Defrost Failure
Ford is recalling 2026 Lincoln Aviator and Explorer vehicles because the HVAC system may fail, causing the windshield defrosting and defogging systems to become inoperative.
Product
FORD — FORD, LINCOLN EXPLORER, AVIATOR
Category
Vehicle
Distribution
Distributed nationwide