The Recall Desk

State

Arizona product recalls

72,936 recalls have nationwide distribution and so reach Arizona. 8,381 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,381
Critical
1,313
Severe
1,717
Most recent
2026-09-09

Of the 8,381 recalls naming Arizona we have scored against our rubric, 1,313 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,717 (20%) are Severe.

These figures cover only the 8,381 recalls whose distribution notice names Arizona specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2376–2400 of 81317

  • HighNHTSA·26V259000·2026-04-22

    Trails West RPM Freeride Recalled for Cooktop Flame Fire Risk

    Trails West is recalling 2027 RPM Freeride recreational trailers because the cooktop flame may invert during furnace operation, increasing fire risk.

    Product
    TRAILS WEST — TRAILS WEST RPM FREERIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1805-2026·2026-04-22

    Philips AneurysmFlow MAFA ratio does not give reliable prognostic information

    Philips is recalling AneurysmFlow because the Mean Aneurysm Flow Amplitude ratio does not reliably predict aneurysm occlusion after flow diverter stent treatment, yet is relied on clinically.

    Product
    Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to be used in combination with a Philips interventional X-ray system and 3DRA data.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1825-2026·2026-04-22

    Philips Spectral CT on Rails recalled over three software issues

    Philips is recalling the Spectral CT on Rails after identifying three software issues affecting gantry movement, a confirmation prompt and head area planning. Three systems are affected.

    Product
    Philips Spectral CT on Rails. Model Number: 728334.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1818-2026·2026-04-22

    Cytal Wound Matrix 10x15 cm recalled over out-of-specification endotoxin results

    Cytal Wound Matrix 2-Layer 10x15 cm dressings are being recalled because of an increased rate of out-of-specification endotoxin results. 452 units are affected.

    Product
    Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0455-2026·2026-04-22

    SLMD benzoyl peroxide acne lotion recalled over benzene contamination

    SLMD Benzoyl Peroxide Acne Lotion, 2.5% benzoyl peroxide, is being recalled because of chemical contamination from the presence of benzene. 2,500 bottles are affected.

    Product
    SLMD Benzoyl Peroxide Acne Lotion, Benzoyl Peroxide 2.5%, a) 0.7 fl. oz - 21 mL and b) 1.5 fl. oz. - 44mL bottles, SANDRA LEE MD., Distributed by Skin PS Brands, Culver City, CA 90232.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0483-2026·2026-04-22

    IMS epinephrine injection vials recalled over lack of sterility assurance

    International Medication Systems is recalling one lot of Epinephrine Injection, USP, 1 mg/10 mL, citing lack of assurance of sterility. 81,520 units are affected.

    Product
    EPINEPHRINE — EPINEPHRINE (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0453-2026·2026-04-22

    HydroPeptide Clear Alliance benzoyl peroxide serum recalled over benzene contamination

    HydroPeptide Clear Alliance Serum, a 2.5% benzoyl peroxide product, is being recalled because of chemical contamination from the presence of benzene. 9,850 bottles are affected.

    Product
    HydroPeptide CLEAR ALLIANCE SERUM, 2.5% BENZOYL PEROXIDE, a)1 FL OZ/30ml; b) 2 FL OZ/60ml spray bottle; DIST BY HYDROPEPTIDE LLC, ISSAQUAH, WA 98027
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1822-2026·2026-04-22

    Cellex photopheresis kit centrifuge bowls may dislodge and break

    Cellex Photopheresis Kits are being recalled because the centrifuge bowl is harder to install and, if fitted improperly, may dislodge and break during priming or treatment.

    Product
    Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a photoimmune therapy where leukocytes are separa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0480-2026·2026-04-22

    glo Skin Beauty Remedy Gel recalled as a subpotent hydrocortisone product

    Remedy Gel, hydrocortisone 1%, distributed by glo Skin Beauty is being recalled because the product is subpotent. The action covers 1,060 bottles.

    Product
    Remedy Gel, hydrocortisone 1%, 30 mL/ 1 fl oz per bottle, Distributed By: glo Skin Beauty, Denver, CO 80216. NDC 66915-531-12; 66915-531-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0481-2026·2026-04-22

    Skin Rehab calming hydrocortisone balm recalled as a subpotent drug

    Skin Rehab Calming Skin Gel Hydrocortisone Balm, hydrocortisone 1%, is being recalled because the product is subpotent. The action covers 2,895 bottles.

    Product
    Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone 1%, .53oz net wt. (15.3g) per bottle, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM. NDC 66915-531-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1810-2026·2026-04-22

    LinkBio CORE Workstation may display an incorrect planning date

    LinkBio is recalling the CORE Workstation, a component of the CORE Shoulder System, because it may display an incorrect planning date on the Start Case menu screen.

    Product
    LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0482-2026·2026-04-22

    Rhonda Allison calming skin gel recalled as a subpotent hydrocortisone product

    Essential Calming Skin Gel containing 1% hydrocortisone is being recalled because the product is subpotent. The action covers 299 bottles.

    Product
    Essential Calming Skin Gel, hydrocortisone 1%, 120mL/4oz net wt. (113g) per jar, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM, NDC 66915-531-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0466-2026·2026-04-22

    Quality Choice sugar free honey lemon cough drops recalled after inspection findings

    QC Quality Choice sugar free Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 25-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON SUGAR FREE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0468-2026·2026-04-22

    Quality Choice honey lemon cough drops recalled after facility inspection findings

    QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0456-2026·2026-04-22

    Exchange Select honey lemon cough drops recalled after facility inspection findings

    Exchange Select Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    HONEY LEMON FLAVOR COUGH DROP — HONEY LEMON FLAVOR COUGH DROP (HONEY LEMON FLAVOR COUGH DROP)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0460-2026·2026-04-22

    Discount Drug Mart menthol cough drops recalled after facility inspection findings

    Discount Drug Mart Food Market Menthol Cough Suppressant Anesthetic Cough Drops, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    DISCOUNT DRUG MART — DISCOUNT DRUG MART (COUGH DROPS MENTHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0459-2026·2026-04-22

    Discount Drug Mart honey lemon cough drops recalled after inspection findings

    Discount Drug Mart Food Market Cough Drops, honey lemon, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    DISCOUNT DRUG MART — DISCOUNT DRUG MART (COUGH DROPS HONEY LEMON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0467-2026·2026-04-22

    Quality Choice strawberry throat drops recalled after facility inspection findings

    QC Quality Choice Pectin Oral Demulcent Throat Soothing Drops, creamy strawberry flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE COUGH DROPS CREAMY STRAWBERRY — QUALITY CHOICE COUGH DROPS CREAMY STRAWBERRY (COUGH DROPS CREAMY STRAWBERRY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0469-2026·2026-04-22

    Quality Choice menthol cough drops recalled after facility inspection findings

    QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, menthol flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS MENTHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0457-2026·2026-04-22

    Menthol Flavor Cough Drops Recalled Due to Potential Product Quality Issues

    Xiamen Kang Zhongyuan Biotechnology Co., Ltd. is recalling Menthol Flavor Cough Drops due to quality concerns identified during an FDA inspection.

    Product
    MENTHOL FLAVOR COUGH DROP — MENTHOL FLAVOR COUGH DROP (MENTHOL FLAVOR COUGH DROP)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0464-2026·2026-04-22

    Quality Choice sugar free black cherry cough drops recalled after inspection findings

    QC Quality Choice sugar free Menthol Cough Suppressant Oral Anesthetic Cough Drops, black cherry, 25-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON SUGAR FREE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0470-2026·2026-04-22

    Quality Choice vanilla honey cough drops recalled after inspection findings

    QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, vanilla honey flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE COUGH DROPS VANILLA HONEY — QUALITY CHOICE COUGH DROPS VANILLA HONEY (COUGH DROPS VANILLA HONEY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0476-2026·2026-04-22

    Taro fluocinonide cream 30 g tubes fail viscosity stability specifications

    Taro is recalling one lot of Fluocinonide 0.05% Cream in 30 g tubes after stability testing returned viscosity results above the specification limit. 41,712 tubes are affected.

    Product
    FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide