The Recall Desk

State

Kentucky product recalls

73,486 recalls have nationwide distribution and so reach Kentucky. 7,202 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total
7,202
Critical
1,409
Severe
2,024
Most recent
2026-10-14

Of the 7,202 recalls naming Kentucky we have scored against our rubric, 1,409 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,024 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,202 recalls whose distribution notice names Kentucky specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22376–22400 of 80688

  • HighFDA (Devices)·Z-1074-2022·2022-05-18

    Phototherapy Units Recalled for Software Bug Causing Incorrect Dosing

    Daavlin's 4 Series CX phototherapy units are recalled due to a software defect that can cause incorrect dosing (over or under) when resuming interrupted treatments.

    Product
    4 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. M4 Ser CX 311-20 120-240V 50/60Hz, item # 807QS0020CX6.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1055-2022·2022-05-18

    Bwell Bird's Nest Lychee Beverage recalled for deficient packaging and spoilage risk

    Eastland Food Corporation is recalling Bwell Bird's Nest Beverage in Lychee Flavor due to deficient packaging material that could lead to premature spoilage. Approximately 1,699 cases were distributed to retail stores across 33 states.

    Product
    Bwell Bird's Nest Beverage Lychee Flavor NET 8.45 FL OZ (250mL) UPC 8373726350 24 bottles per case
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-1072-2022·2022-05-18

    Radial Head Replacement System implant: contraindications added to safety instructions

    Synthes has updated safety instructions for its Radial Head Replacement System implant with absolute contraindications for use in patients with infection, sepsis, or osteomyelitis. The FDA has classified this as a Class II recall.

    Product
    Radial Head Replacement System Implant is a one-piece, stemmed radial head replacement. The radial head is available in diameters of 19, 22 and 25mm. The radial stems range from 5.5 to 8.5mm in diameter and from 21 24mm in length.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1071-2022·2022-05-18

    TMJ Arthroscopy Drape incorrectly labeled latex-free when containing latex

    Microtek Medical Inc. is recalling TMJ Arthroscopy Drapes that contain latex but were mislabeled as latex-free, posing an allergic reaction risk to patients and healthcare workers with latex sensitivities.

    Product
    TMJ Arthroscopy Drape, 85''x 96''
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2022·2022-05-18

    Spine Surgery Instrument Sets Recalled for Sterilization Defect

    American Contract Systems is recalling ACS Spine Pack and ACS Lumbar/Back Set Up Tray surgical instrument sets due to improper sterilization with excess ethylene oxide. The affected sets were distributed in Illinois, Missouri, Nebraska, and Texas.

    Product
    1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1070-2022·2022-05-18

    Flexible video uretero-renoscopes recalled for inadequate sterilization

    Karl Storz Endoscopy is recalling Flexible Video-Uretero-Renoscope (FLEX-XC) models because they may fail to achieve adequate disinfection, creating potential microbial contamination risk.

    Product
    11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSE 11278VSEK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSU 11278VSUK Flexible Video-Uretero-Renoscope (FLEX-XC) Z18447US-BC (03/2018); 11278VSUA 11278VSUAK…
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1063-2022·2022-05-18

    Karl Storz HD Cysto-Urethroscope recalled for disinfection failure

    Karl Storz is recalling HD-VIEW Flexible HD Cysto-Urethroscope models that fail to adequately disinfect during processing, creating a potential infection risk. All units manufactured since January 2018 are affected.

    Product
    11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC (10-2021) 11272VHU-TL 11272VHUK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC (10-2021)
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1054-2022·2022-05-18

    KARL STORZ Nasopharyngolaryngoscope Disinfection Failure Affects 14 States

    The FDA is recalling KARL STORZ Slim Nasopharyngolaryngoscope models 11001RD1 and 11001RDK1 because they fail to achieve adequate disinfection, potentially allowing microorganisms to persist on the device and transmit between patients.

    Product
    11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1066-2022·2022-05-18

    Flexible Cystoscopes Recalled for Inadequate Disinfection Process

    Karl Storz Flexible Cystoscope units may not be properly disinfected because the disinfection process fails to achieve the expected reduction of microorganisms. All units manufactured since January 2018 are potentially affected.

    Product
    11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018)
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1038-2022·2022-05-18

    ACS IR Angio Pack Sterilization Process Defect Recall

    The ACS IR Angio Pack from American Contract Systems, Inc. was sterilized using ethylene oxide at higher than specification concentration. No illnesses or injuries have been reported.

    Product
    ACS IR - Angio Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0860-2022·2022-05-18

    Esomeprazole magnesium delayed-release capsules recalled for impurity specification failure

    Mylan Institutional Inc. is recalling Esomeprazole Magnesium Delayed-Release Capsules 20 mg due to failed impurity specifications detected during stability testing. 555 cartons of affected lots were distributed nationwide.

    Product
    Esomeprazole Magnesium Delayed-Release Capsules, USP 20 mg, packaged in Unit Dose Blister Cards of 6 (10 cards of 6 Capsules each per carton), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC 42292-009-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1073-2022·2022-05-18

    Daavlin 1 Series CX Phototherapy Units Recalled for Software Dosing Error

    Daavlin is recalling 1 Series CX phototherapy units due to a software bug that swaps calibration distance settings when resuming interrupted treatments, resulting in incorrect dosing.

    Product
    1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. Models: [1 Ser CX 305-4 120-240V 50/60Hz, item # 06OS0004CX6], [1 Ser CX 311-4 120-240V 50/60Hz CE, item # 807OS0004CX5], [1 Ser CX 311-4 120-240V 50/60Hz, item…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1075-2022·2022-05-18

    X-ray Imaging Systems Have Reversed Spine Positioning Labels

    Shanghai United Imaging's digital X-ray systems may display reversed spine positioning labels, potentially causing misdiagnosis and unnecessary repeat radiation exposure for patients.

    Product
    Digital Medical X-ray Imaging System, Model: uDR 596i, uDR 592h
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1064-2022·2022-05-18

    Karl Storz Flexible Video Urethro Cystoscope Recalled for Inadequate Disinfection

    Karl Storz is recalling multiple Flexible Video Urethro Cystoscope models because they may fail to achieve proper disinfection between procedures, posing a risk of microbial contamination.

    Product
    11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018); 11272VNU 11272VNUK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1065-2022·2022-05-18

    Cysto-Urethroscope Disinfection Process Failure Affects Serial Numbers Since 2018

    Karl Storz Endoscopy is recalling Flexible Video Cysto-Urethroscopes due to a disinfection process failure that may not adequately eliminate microorganisms. Affected units have been distributed nationwide and internationally since January 2018.

    Product
    11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1 (04/2021); 11272VUE-R 11272VUEK-R Flexible Video Cysto-Urethroscope 96136031USCA V1.1 (04/2021)
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1047-2022·2022-05-18

    Bronchovideoscope Reprocessing Instructions Updated Due to Sterilization Concerns

    Olympus is issuing updated instructions for reprocessing its EVIS EXERA bronchovideoscopes to ensure proper sterilization and disinfection procedures. Improper reprocessing could compromise device safety.

    Product
    BF-3C160: EVIS EXERA Bronchovideoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1067-2022·2022-05-18

    Flexible Ureteroscope Recall Due to Inadequate Disinfection Process

    Karl Storz Endoscopy is recalling flexible ureteroscopes manufactured or distributed since January 2018 due to the disinfection process failing to achieve expected microbial reduction levels.

    Product
    11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018); 11278AC1 N/A Flexible Ureteroscope Z17859US-A (04/2016); 11278AC2 11278ACK2 Flexible Ureteroscope Z20615US-BA (08-2018); 11278ACU1 11278ACUK1 Flexible Ureteroscope Z20615US-BA (08-2018); 11278AU1 11278AUK1…
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1069-2022·2022-05-18

    Flexible Uretero-Renoscopes Recalled for Inadequate Disinfection

    Karl Storz Endoscopy is recalling Flexible Video-Uretero-Renoscope instruments due to inadequate microbial disinfection. All units manufactured since January 2018 are affected.

    Product
    11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSE 11278VSEK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSU 11278VSUK Flexible Video-Uretero-Renoscope (FLEX-XC) Z18447US-BC (03/2018); 11278VSUA 11278VSUAK…
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1048-2022·2022-05-18

    Bronchofibervideoscope Sterilization and Disinfection Procedure Update Recall

    Olympus is recalling 292 units of the BF-MP160F EVIS EXERA Bronchofibervideoscope due to updated instructions required for proper sterilization and reprocessing procedures. Updated guidance for chemical reprocessing, ETO gas sterilization, and disinfection rinsing steps is necessary.

    Product
    BF-MP160F: EVIS EXERA Bronchofibervideoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V347000·2022-05-18

    Prevost Recalls X3-45 Commuter Vehicles Due to Rearview Mirror Defect

    Prevost is recalling 2020-2022 X3-45 Commuter vehicles because the right-side rearview mirror is positioned incorrectly, obstructing the driver's view and increasing crash risk.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1061-2022·2022-05-18

    Karl Storz cystoscopes recalled due to inadequate disinfection

    Karl Storz cystoscopes manufactured since January 2018 are recalled because they may not achieve required disinfection levels. Inadequate disinfection could lead to patient infection during urological procedures.

    Product
    CYSTO-URETHRO-FIBERSCOPE REF 11272C1 CYSTOSCOPE, 15FR X 370MM, ADULT REF 11272C2 and Kit Number 11272CK2 CYSTO-URETHRO-FIBERSCOPE REF 11272CU1 and Kit Number 11272CUK1
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1050-2022·2022-05-18

    FDA Recalls Unauthorized COVID-19 Antigen Rapid Test Kits

    USA Medical, LLC distributed 2055 COVID-19 antigen test kits nationwide. The tests did not receive FDA Emergency Use Authorization nor were they cleared or approved for commercial distribution.

    Product
    Diagnostic Kit SARS-cCo V Antigen Rapid Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V348000·2022-05-18

    Airstream Travel Trailers: Manual Step May Collapse Due to Fastener Defect

    Airstream is recalling certain 2022-2023 travel trailers with manual steps that may collapse due to a fastener screw pulling through the washer, increasing the risk of injury.

    Product
    AIRSTREAM — AIRSTREAM INTERNATIONAL, POTTERY BARN, GLOBETROTTER, FLYING CLOUD
    Category
    Vehicle
    Distribution
    Distributed nationwide