State

Kentucky product recalls

73,584 recalls have nationwide distribution and so reach Kentucky. 7,203 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total: 7,203
Critical: 1,407
Severe: 2,026
Most recent: 2026-10-21

Of the 7,203 recalls naming Kentucky we have scored against our rubric, 1,407 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,026 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,203 recalls whose distribution notice names Kentucky specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26951–26975 of 80787

HighFDA (Devices)·Z-1683-2021·2021-06-02
Radiometer Recalls PICO70 Arterial Blood Samplers Due to Sterile Barrier Breach
Radiometer is recalling PICO70 Arterial Blood Samplers because a sterile barrier breach was found during testing, posing a risk of bacterial infection.
Product
PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized, electrolyte-balanced, arterial blood sampler product line for collection of arterial samples for pH, blood gas, oximetry, electrolyte and metabolite analysis. Model Number/Product Description: 956-518…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1672-2021·2021-06-02
Welch Allyn GS777 Wall Transformer Recalled for Electrical Shock Risk
Welch Allyn is recalling GS777 Wall Transformers due to a potential risk of fluid ingress causing electrical shorts and shock.
Product
GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulatory and acute care settings.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V413000·2021-06-02
2021 Volkswagen ID.4 recalled for incorrect headlight aiming caps
Volkswagen is recalling certain 2021 ID.4 vehicles because headlight aiming caps were installed on the vertical adjustment instead of the horizontal adjustment. This defect can increase glare and reduce visibility, increasing the risk of a crash.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0627-2021·2021-06-02
Brill Inc Recalls Jumbo Chocolate Chip Cookies Due to Foreign Objects
Brill Inc is recalling Jumbo Chocolate Chip Cookies nationwide because they may contain small foreign objects.
Product
10233579 JUMBO CHOCOLATE CHIP COOKIE 12 / 12 INCH BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN Net weight: 17.04 lb (7.73 kg)
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1670-2021·2021-06-02
Beckman Coulter Access SARS-CoV-2 Antigen Recalled for False Negative Risk
Beckman Coulter is recalling Access SARS-CoV-2 Antigen test kits because specimens stored in certain conditions may yield false negative results.
Product
Access SARS-CoV-2 Antigen, REF C68668, UDI: (01)15099590742713, 3.30 mL/R1a, 4.70 mL/R1b, 4.20 mL/R1c, 3.10 mL, R1d, 3.10 mL, R1e
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V416000·2021-06-02
Mack 2021-2022 trucks recalled for hubcap separation hazard
Mack Trucks is recalling 307 certain 2021-2022 Granite, Pinnacle, and Anthem commercial trucks due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard and increasing crash risk.
Product
MACK — MACK PINNACLE (CHU), PINNACLE (CXU), ANTHEM (AN), GRANITE (GR)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V410000·2021-06-02
Mercedes-Benz Sprinter Recall for Swivel Seat Wiring Harness Defect
Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans with swivel seats because incorrect wiring harness routing may damage the seat air bag system.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 4500, SPRINTER 3500, SPRINTER 1500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V412000·2021-06-02
Sutphen Recalls 2019-2020 Fire Trucks Due to Wireless Controller Battery Issue
Sutphen is recalling 2019-2020 fire trucks because a disabled sleep mode causes the wireless remote controller's batteries to discharge faster than normal.
Product
SUTPHEN — SUTPHEN FIRE TRUCK
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1682-2021·2021-06-02
Pentax Medical Video Duodenoscope Recalled for Distal End Cap Detachment Risk
Pentax of America Inc. is recalling 108 Pentax Medical Video Duodenoscopes because the distal end cap may detach during procedures, posing risks of injury or aspiration.
Product
Pentax Medical Video Duodenoscope - Product Usage: intended to be used with endoscopic devices and other ancillary equipment to provide optical visualization of (via a video monitor), and therapeutic access to, Biliary Tract via the Upper Gastrointestinal Tract, Model Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1673-2021·2021-06-02
Welch Allyn ProBP 3400 Digital Blood Pressure Device Recall
Welch Allyn is recalling ProBP 3400 Digital Blood Pressure Devices due to a risk of fluid ingress causing electrical shorts and potential shock.
Product
ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34XFHT-B Intended: ProBP 3400 automatically measures systolic and diastolic pressure (excluding neonates) and pulse rate, as well as calculates Mean Arterial Pressure (MAP).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1687-2021·2021-06-02
James Leckey MyWay Walker Chassis Recalled Due to Weld Failure
James Leckey Design Ltd is recalling 2,719 MyWay Walker Chassis units because weld failures caused casters to detach from the rear legs.
Product
MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1676-2021·2021-06-02
Dentech Corp. Recalls Rubber Dam Clamps Due to Possible Breakage
Dentech Corp. is recalling 87,842 units of KSK Rubber Dam Clamps because they may break during use. The recall covers units distributed in the US and worldwide.
Product
Rubber Dam Clamp, KSK - Product Usage: used for prevention of contamination by saliva and moisture prevention during dental treatment.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V411000·2021-06-02
Mercedes-Benz and Freightliner Sprinter Recalled for Rearview Camera Software Defect
Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans because a software defect may cause the rearview camera image to fail to display.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 1500, SPRINTER 3500, SPRINTER 4500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1671-2021·2021-06-02
Philips IntelliVue MX40 Patient Monitor Recalled for Manufacturing Defects
Philips is recalling three IntelliVue MX40 patient monitors because manufacturing process failures may have resulted in defective devices.
Product
IntelliVue MX40 Patient Monitor, Model Number: 865350 (US) 865352 (OUS) Software version number B.06.59 - Product Usage: Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and…
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-06022021·2021-06-02
USDA Issues Public Health Alert for Raw Breaded Stuffed Chicken Products
USDA FSIS issued a public health alert for frozen raw breaded stuffed chicken products due to a Salmonella Enteritidis illness cluster. Consumers are advised to cook products to 165 F.
Product
FSIS Issues Public Health Alert for Frozen Raw Breaded Stuffed Chicken Products Due to Possible Salmonella Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·21V417000·2021-06-02
Volvo Trucks recalls 2021-2022 vehicles for hubcap separation hazard
Volvo Trucks is recalling certain 2021-2022 VAH, VDH, VNL, and VNR vehicles due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard. Dealers will remove the hubcap free of charge.
Product
VOLVO — VOLVO VNL, VAH, VHD, VNR
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1679-2021·2021-06-02
Nobel Biocare Implant Crown Recalled for Manufacturing Specification Defects
Nobel Biocare Procera LLC is recalling specific implant crown units because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77363
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1675-2021·2021-06-02
Roche Recalls Iron Gen 2 Reagent Cassettes Due to Discrepant Results
Roche Diagnostics is recalling 20,468 Iron Gen 2 reagent cassettes because they may produce discrepant elevated results on specific analyzers.
Product
IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for the quantitative determination of iron in human serum and plasma on Roche/Hitachi cobas c and cobas Integra systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1681-2021·2021-06-02
Nobel Biocare Procera LLC Recalls Implant Crowns Not Manufactured to Specification
Nobel Biocare Procera LLC is recalling specific implant crowns because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77387
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1674-2021·2021-06-02
Siemens Centaur Syphilis Assay Recalled for Potential Carryover Interference
Siemens Healthcare Diagnostics is recalling the Centaur Syphilis Assay-SYP Kit due to potential carryover into other assays on specific systems.
Product
Centaur Syphilis Assay-SYP Kit, 200 Test - Product Usage: For in vitro diagnostic use in the qualitative determination of antibodies to Treponema pallidum in human serum or plasma using the ADVIA Centaur XP/XPT System and ADVIA Centaur CP Systems, SMN:10492493
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0394-2021·2021-06-02
Noven Recalls Daytrana Methylphenidate Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because customer complaints regarding ripped patches and adhesive transfer exceeded action limits.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1678-2021·2021-06-02
Nobel Biocare Procera Implant Crown Recall for Manufacturing Defects
Nobel Biocare Procera LLC is recalling seven implant crown units because they were not manufactured to specification. The recall covers distribution in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77352
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0564-2021·2021-06-02
Brew Dr. Uplift Drink Recalled Due to Yeast Presence
Brew Dr. Uplift Blood Orange Lemon drink is being recalled because yeast was found in the shelf-stable cans.
Product
Brew Dr. Uplift Blood Orange Lemon, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00870 9. The label is read in parts: "***BLOOD ORANGE LEMON *** YERBA MATE * GUAYUSA * GREEN TEA***BREW DR. UPLIFT…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0563-2021·2021-06-02
Brew Dr. Uplift Blueberry Raspberry Yerba Mate Recalled for Yeast
Brew Dr. Uplift Blueberry Raspberry Yerba Mate is being recalled because yeast was found in the shelf-stable cans.
Product
Brew Dr. Uplift Blueberry Raspberry Yerba Mate Guayusa, Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00867 9. The label is read in parts: "***BLUEBERRY RASPBERRY ***YERBA MATE * GUAYUSA * GREEN TEA***BREW DR UPLIFT ***…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0565-2021·2021-06-02
Brew Dr. Uplift Mango Passionfruit Recalled for Yeast Contamination
Brew Dr. Uplift Mango Passionfruit drinks are being recalled because yeast was found in the product. Consumers should stop drinking the affected cans.
Product
Brew Dr. Uplift Mango Passionfruit, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00871 6. The label is read in parts: "***MANGO PASSIONFRUIT *** YERBA MATE * GUAYUSA * GREEN TEA *** BREW DR. UPLIFT…
Category
Food
Distribution
Distributed nationwide