The Recall Desk

State

Kansas product recalls

72,907 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,723
Critical
1,045
Severe
1,228
Most recent
2026-09-02

Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.

These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1276–1300 of 78630

  • ModerateFDA (Drugs)·D-0634-2026·2026-06-24

    Cura Hongos clotrimazole cream recalled over manufacturing practice deviations

    Cura Hongos Crema Antifungica, clotrimazole 1%, in 2 oz tubes is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 84 tubes affected.

    Product
    Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 52924 00683 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2419-2026·2026-06-24

    Medline central line dressing and port kits contain recalled Mastisol

    Medline central line dressing kits, PICC/CVC/midline CHG dressing kits, port-a-cath kits and vein ablation packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2448-2026·2026-06-24

    HarmonyAIR A-Series surgical light heads may show paint delamination

    HarmonyAIR A-Series Surgical Lighting Systems are being recalled because of the potential for paint delamination, meaning chipping or peeling, on the light heads. 4,138 units affected.

    Product
    HarmonyAIR A-Series Surgical Lighting System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2422-2026·2026-06-24

    Medline abdominal and bariatric packs contain recalled Mastisol liquid adhesive

    Medline convenience kits including abdominal, bariatric and laparoscopic cholecystectomy packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS CDS983883J BWNBORO LAP CHOLE PACK-LF DYNJ32836B CCSB KARIN JWIRE LUMPECTOMY DYNJ910459B CHRISTUS CHILDRENS LAP CHOLE DYNJ61165G CUH MINOR PACK-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0630-2026·2026-06-24

    Lucky Super Soft triple antibiotic ointment recalled over manufacturing deviations

    Lucky Super Soft First Aid Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 2,503 tubes are affected.

    Product
    Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 units, neomycin sulphate 3.5 mg, polymyxin B sulphate 5000 units, Net Wt. 0.5 oz (14g) tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0631-2026·2026-06-24

    Circle K triple antibiotic ointment recalled over manufacturing practice deviations

    Circle K Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 2,420 tubes are affected.

    Product
    Circle K, triple antibiotic ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g) tubes, Product manufactured for Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404, Made in India, UPC
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2444-2026·2026-06-24

    Medline vascular and cardiac packs contain recalled Mastisol liquid adhesive

    Medline convenience kits including AV fistula, endovascular, EP device and aneurysm packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672P GEN FEM POP #14-RF DYNJ21877W IMPLANT PACK DYNJ39316D OPEN HEART MR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2436-2026·2026-06-24

    Medline ACDF and ACL procedure kits contain recalled Mastisol adhesive

    Medline convenience kits for ACD, ACDF, ACL and ALIF procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996 ACL ACCESSORY PACK DYNJ86584B ACL- LF DYNJ905281B ACL PACK DYNJ67271A ALIF DYNJ904848L ANTERIOR CERVICAL DYNJ901355J ARTHROSCOPY DYN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2427-2026·2026-06-24

    Medline hernia repair totes contain recalled Mastisol liquid adhesive

    The Medline Hernia Repair Tote convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0640-2026·2026-06-24

    Med Pride hydrocortisone cream 1oz tubes recalled over manufacturing deviations

    Med Pride Hydrocortisone Cream 1%, 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,944 tubes are affected.

    Product
    Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 1 oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30503 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2423-2026·2026-06-24

    Medline plastic surgery kits contain recalled Mastisol liquid adhesive

    Medline convenience kits for breast imaging, plastics and facial procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A ENDO BREAST AUGMENTATION PACK DYNJ68023 FACIAL PLASTIC DYNJ909926C JVL - MODULE PLASTIC PK DYNJ84081B KIT MAJOR PLASTICS MOSES DYNJ905362C MEM MAXILLOFACIAL PACK-LF DYNJ0660040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0588-2026·2026-06-24

    Alyacen 7/7/7 birth control tablets failed total impurities specification

    Alyacen 7/7/7 norethindrone and ethinyl estradiol tablets are being recalled because of out-of-specification results for total impurities.

    Product
    ALYACEN 1/35 — ALYACEN 1/35 (NORETHINDRONE AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2429-2026·2026-06-24

    Medline labor and delivery C-section kits contain recalled Mastisol adhesive

    The Medline Labor & Delivery C-Section convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0603-2026·2026-06-24

    Burkhart benzocaine topical anesthetic gel bottles may have incomplete seals

    Burkhart topical anesthetic gel, benzocaine 20% strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 150 units are affected.

    Product
    BURKHART TOPICAL ANESTHETIC — BURKHART TOPICAL ANESTHETIC (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2431-2026·2026-06-24

    Medline da Vinci and gynaecology laparoscopy kits contain recalled Mastisol

    Medline da Vinci, general robotics and gynaecology laparoscopy convenience kits are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2416-2026·2026-06-24

    Medline block trays and indwelling nerve blocks contain recalled Mastisol

    The Medline Block Tray and Indwelling Nerve Block kit are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2433-2026·2026-06-24

    Medline LAVH packs contain recalled Mastisol liquid adhesive

    The Medline WT LAVH Pack is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kits: WT LAVH PACK DYNJ46609F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2418-2026·2026-06-24

    Medline pacemaker and open heart packs contain recalled Mastisol adhesive

    Medline convenience kits including pacemaker, ICD, open heart and pediatric open heart packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C PACEMAKER PK DYNJT3454 PACEMAKER/ICD PACK DYNJ33822L PAD OPEN HEART DYNJ900962O PEDIATRIC OPEN HEART DYNJ54238L DYNJT6766 STAZ BASIC VASCULAR DYNJ909794C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2460-2026·2026-06-24

    directCHECK whole blood control labeled with incorrect performance range

    directCHECK ACT-LR whole blood quality control, level 2, is being recalled because the assayed control carries labeling with an incorrect performance range. 6,060 units affected.

    Product
    directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0602-2026·2026-06-24

    DHP benzocaine topical anesthetic gel bottles may have incomplete seals

    DHP Topical Anesthetic Gel, benzocaine 20% strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 150 units are affected.

    Product
    HEALTH-TEC TOPICAL ANESTHETIC — HEALTH-TEC TOPICAL ANESTHETIC (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0639-2026·2026-06-24

    Med Pride hydrocortisone cream 16oz tubes recalled over manufacturing deviations

    Med Pride Hydrocortisone Cream 1%, 16 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,738 tubes are affected.

    Product
    Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 16oz (454g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 305061.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2449-2026·2026-06-24

    HarmonyAIR A-Series surgical light intensity control buttons may detach

    HarmonyAIR A-Series Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 2,101 units affected.

    Product
    HarmonyAIR A-Series Surgical Lighting System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0637-2026·2026-06-24

    Med Pride bacitracin zinc ointment recalled over manufacturing practice deviations

    Med Pride Bacitracin Zinc Ointment, 1 oz tubes, is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 1,185 tubes affected.

    Product
    Med Pride, Bacitracin Zinc Ointment, 1oz (28.3g) per tube, 72 tubes per case, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC X004WB4LKT.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2450-2026·2026-06-24

    ALYON surgical light head intensity control buttons may detach

    ALYON Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 549 units are affected.

    Product
    ALYON Surgical Lighting System
    Category
    Medical Device
    Distribution
    Distributed nationwide