The Recall Desk

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.

26976–27000 of 80787

  • ModerateFDA (Devices)·Z-1688-2021·2021-06-02

    Ortho VITROS CoV2 Ag Calibrator Recalled for Calibration Failures

    Ortho-Clinical Diagnostics is recalling 74 units of VITROS CoV2 Ag calibrator (Lot 0020) due to potential unexpected calibration failures.

    Product
    VITROS CoV2 Ag calibrator (Product Code 6199950) - Product Usage: is a chemiluminescent immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigens in nasopharyngeal (NP) and anterior nasal swab specimens collected in CDCs formulation of VTM.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0628-2021·2021-06-02

    Brill Inc Recalls Chocolate Chip Cookies for Potential Foreign Objects

    Brill Inc is recalling specific batches of baked chocolate chip cookies due to the potential presence of small foreign objects.

    Product
    10239710: 12" BAKED CHOCOLATE CHIP MESSAGE COOKIE 14 / 22 oz BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN AT 0¿F OR BELOW Net weight 19.25 lb (8.73 kg) (14 x 22 oz (624g)) and 10239711 9" CHOCOLATE CHIP BAKED MESSAGE COOKIE 16 / 12.5 oz BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN AT…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1680-2021·2021-06-02

    Nobel Biocare Procera Implant Crown Recalled for Manufacturing Defect

    Nobel Biocare Procera LLC is recalling specific implant crown units that were not manufactured to specification. The recall affects units distributed in the US and several international countries.

    Product
    NPr FCZ¿Imp Crwn ASC CC RP 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: 77364
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0393-2021·2021-06-02

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because customer complaints regarding ripped patches and adhesive issues exceeded action limits.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1677-2021·2021-06-02

    Nobel Biocare Procera Recalls Two Dental Implant Crowns for Specification Defects

    Nobel Biocare Procera LLC is recalling two dental implant crown units because they were not manufactured to specification. The affected units were distributed in the US and several international countries.

    Product
    NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - 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: 77339
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0392-2021·2021-06-02

    Ascend Recalls Olmesartan Medoxomil Tablets Due to Foreign Tablet Presence

    Ascend Laboratories LLC is recalling 34,296 bottles of Olmesartan Medoxomil 20 mg tablets because they may contain a foreign tablet or capsule.

    Product
    OLMESARTAN MEDOXOMIL — OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0599-2021·2021-06-02

    Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 10 mg tablets due to the presence of degradation impurities.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·21V409000·2021-06-01

    Altec Aerial Devices Recalled for Boom Spool Shift Risk

    Altec is recalling 2005-2021 aerial devices because boom spools can shift, increasing injury risk. Owners should contact Altec for free repairs.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V408000·2021-06-01

    Custom Truck Recalls 2020 Ford F-550 Vehicles Due to Display Defect

    Custom Truck is recalling 2020 Ford F-550 vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    CUSTOM TRUCK & BODY WORKS — CUSTOM TRUCK & BODY WORKS FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V407000·2021-05-29

    Ford Recalls 2021 F-150 Trucks Due to Steering Gear Defect

    Ford is recalling 2021 F-150 vehicles because internal steering gear damage could cause loss of steering control. Owners should not drive until the repair is complete.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V406000·2021-05-28

    2021 Mercedes-Benz Cabriolets: Rear Headrests May Be Incorrectly Mounted

    Mercedes-Benz USA is recalling approximately 218 2021 Cabriolet models due to rear headrests that may be incorrectly mounted to the seatbacks. The headrests could move or detach during a crash, increasing the risk of injury.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, E 450, AMG E53, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V403000·2021-05-28

    Mercedes-Benz Recalls 2020 GLB 250 Vehicles for Water Intrusion Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because water may enter the foot wells, potentially causing electrical damage, engine stalls, or a blank instrument cluster.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V405000·2021-05-28

    Mercedes-Benz Recalls 2020 GLB 250 Vehicles for Air Bag Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because the front passenger air bag may tear upon deployment, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V404000·2021-05-28

    Mercedes-Benz Recalls 2020 GLB 250 for Side Air Bag Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because side curtain air bags may not deploy properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V401000·2021-05-27

    BMW Recalls 3 Series Vehicles for Air Bag Inflator Defect

    BMW is recalling 1999-2001 3 Series vehicles because the driver-side air bag inflator may explode or underinflate, posing a risk of serious injury.

    Product
    BMW — BMW 330CI, 3 SERIES, 328CI, 330I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V402000·2021-05-27

    2021 INFINITI QX50 Steering Knuckle Structural Defect - Multiple Models Affected

    Nissan recalls 2021 INFINITI QX50 and other vehicles due to front steering knuckles and rear axle housings with insufficient strength from improper heat treatment, which could deform on impact and cause loss of steering control or wheel separation.

    Product
    INFINITI — INFINITI, NISSAN QX60, MURANO, Q50, GT-R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V400000·2021-05-27

    Triple E RV Recalls 2020-2021 Models Due to Refrigerator Exhaust Deflector Issue

    Triple E Recreational Vehicles is recalling 2020-2021 Serenity, Unity, and Wonder models because a low-positioned metal deflector allows exhaust to char the wood frame, increasing fire risk.

    Product
    TRIPLE E RV — TRIPLE E RV, TRIPLE E WONDER, SERENITY, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V398000·2021-05-27

    RAM 3500, 4500, and 5500 vehicles recalled for wheel stud failure

    Chrysler is recalling RAM trucks because incorrect manual torque specifications can cause wheel studs to over-tighten, break, and lead to wheel separation and possible crashes.

    Product
    RAM — RAM, DODGE 5500, 3500, 4500, RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21751·2021-05-27

    Umbrosa Pool and Patio Umbrellas Recalled Due to Arm Breakage Hazard

    Umbrosa is recalling about 250 pool and patio umbrellas because the arm can break at the elbow while in use, posing an injury hazard.

    Product
    Umbrosa umbrellas equipped with the Umbrosa Evolution Arm/Holder
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21750·2021-05-27

    Williams Advanced Materials Recalls Three Chemicals for Packaging and Labeling Violations

    Williams Advanced Materials & Chemicals is recalling sodium hydroxide, heptane, and naphtha because the packaging is not child-resistant and labels violate federal requirements.

    Product
    Williams Advanced Materials & Chemicals Recalls Three Chemical Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement (Recall Alert)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0503-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Isolate for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE NEOPOLITAN ICE CREAM DIETARY SUPPLEMENT NET WT. 2lb, UPC 8 11836 02251 3 & 5lb, UPC 8 11836 02252 0 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • CriticalFDA (Food)·F-0539-2021·2021-05-26

    Natural Way Almond Butter Recalled for Potential Undeclared Peanuts

    Simkins Brothers Sweets is recalling Natural Way Almond Butter due to potential undeclared peanuts. Consumers should check for lot #505721.

    Product
    Natural Way Almond Butter 16 oz. UPC 850001775175 packaged in clear plastic jars
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0501-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89001 0 & 5lb, UPC 6 49241 87831 5 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states