The Recall Desk

State

Arizona product recalls

73,106 recalls have nationwide distribution and so reach Arizona. 8,386 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,386
Critical
1,313
Severe
1,720
Most recent
2026-10-02

Of the 8,386 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 1,720 (21%) are Severe.

Which agencies issued them

These figures cover only the 8,386 recalls whose distribution notice names Arizona specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12726–12750 of 81492

  • ModerateFDA (Drugs)·D-0433-2024·2024-04-10

    Cyclophosphamide Injection Recalled for Package Insert Concentration Labeling Error

    X-Gen Pharmaceuticals is recalling 1,283 vials of Cyclophosphamide for Injection due to a Package Insert error that lists concentration as '20 mg per vial' instead of '20 mg per mL'. No illnesses have been reported.

    Product
    Cyclophosphamide for Injection, USP, 500mg/vial, Lyophilized, Cytotoxic Agent, Single Dose Vial for Intravenous Use, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc. Big Flats, NY 14814, NDC # 39822-0250-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0434-2024·2024-04-10

    Cyclophosphamide Injection Recalled for Package Insert Concentration Labeling Error

    X-Gen Pharmaceuticals recalls Cyclophosphamide for Injection due to a labeling error in the Package Insert. Section 2.3 incorrectly lists the concentration as '20 mg per vial' instead of the correct '20 mg per mL'.

    Product
    Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After Reconstitution: For direct intravenous injection or must be further diluted before intravenous infusion, Rx Only, Manufactured for: XGen Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V253000·2024-04-05

    Forest River Recalls Transit Buses Due to Unsecured Brake Lines

    Forest River Bus is recalling specific 2018-2024 transit bus models because unsecured brake lines may be damaged by the frame rail, increasing crash risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, ELDORADO, ELKHART SENATOR II, CANDIDATE II, ADVANTAGE, ALLSTAR MVP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V080000·2024-04-05

    Autocar Recalls 2023 Xpeditor and Xspotter Vehicles for Steering Defect

    Autocar is recalling 2023 Xpeditor and Xspotter vehicles because steering gears may have fewer recirculating balls than required, risking loss of steering control.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V254000·2024-04-05

    2024 Coachmen Catalina and Aurora Travel Trailers: Electrical Fire Risk

    Forest River is recalling certain 2024 Coachmen Catalina and Aurora Travel Trailers due to improper routing of the distribution panel wire. The unprotected wire increases the risk of fire.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN AURORA, CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V255000·2024-04-05

    Aston Martin DBX electrical cable defect may cause engine stall

    Aston Martin is recalling 2021-2024 DBX vehicles due to loose electrical cables in the battery fuse box, which may cause engine stall, loss of headlights, or loss of power steering, increasing crash risk.

    Product
    ASTON MARTIN — ASTON MARTIN DBX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24189·2024-04-05

    Procter & Gamble Recalls 8.2 Million Defective Laundry Detergent Packet Bags

    Procter & Gamble is recalling about 8.2 million bags of Tide, Gain, Ace, and Ariel laundry detergent packets because the outer packaging can split open near the zipper, risking serious injury, ingestion, or skin or eye injuries—especially to children.

    Product
    Tide Pods, Gain Flings, Ace Pods and Ariel Pods liquid laundry detergent packets packaged in flexible film bags. This recall announcement applies only to bags distributed in the United States.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·24180·2024-04-04

    C2 Crank Cocking Aids for Excalibur Crossbows Recalled for Impact Injury and Laceration Hazards

    Excalibur Crossbow is recalling about 15,000 C2 Crank cocking aids because the plastic cocking hooks can break during use and become flying projectiles, causing impact injuries and lacerations. One consumer reportedly suffered a permanent eye injury.

    Product
    C2 Crank Cocking Aid for Crossbows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·24179·2024-04-04

    Essential Medical Supply Reannounces Adult Bed Rails Recall; Entrapment and Asphyxia

    Essential Medical Supply is reannouncing a recall of approximately 272,000 Endurance® Hand Bed Rails due to entrapment and asphyxiation hazards. Two additional deaths have been reported since the original 2021 recall.

    Product
    Endurance® Hand Bed Rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·24181·2024-04-04

    BLACK+DECKER Garment Steamers Recalled Nationwide for Burn Hazard

    Empower Brands is recalling approximately 1.6 million BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, causing burn injuries. Consumers should stop using the steamers immediately and contact the manufacturer for a full refund.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V252000·2024-04-04

    Terex Advance Recalls 2023 Commander Vehicles for Steering Defect

    Terex Advance is recalling 2023 Commander vehicles because steering components may not be installed correctly, increasing the risk of a crash.

    Product
    TEREX ADVANCE — TEREX ADVANCE COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24184·2024-04-04

    Zazaba International Recalls Grão de Gente Baby Nests for Suffocation and Fall Hazards

    Zazaba International is recalling about 430 Grão de Gente baby nests sold online from March 2023 through August 2023 due to suffocation risk and fall and entrapment hazards that violate federal infant sleep product safety standards.

    Product
    Grão de Gente Baby Nests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24178·2024-04-04

    Walmart Recalls Mainstays Electric Mini Choppers for Laceration Hazard

    Walmart is recalling about 51,750 Mainstays Electric Mini Choppers because the blade can operate unexpectedly during assembly or when not enclosed, causing cuts. Five lacerations have been reported, two requiring medical attention.

    Product
    Mainstays Electric Mini Choppers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24185·2024-04-04

    Zazaba International Recalls Grão de Gente Crib Bumper Bedding Sets for Suffocation Risk

    Zazaba International is recalling about 795 Grão de Gente padded crib bumper bedding sets sold online between March and August 2023 due to suffocation hazard. Infants can suffocate if they roll into the bumper, which violates the federal Safe Sleep for Babies Act of 2021.

    Product
    Grão de Gente Crib Bumper Bedding Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24183·2024-04-04

    Children's Two-Piece Pajamas and Lounge Dresses Flammability Violation Recall

    Koala Tree Enterprises (DBA Lovey & Grink) is recalling approximately 23,720 children's two-piece pajamas and lounge dresses because they violate federal flammability regulations for children's sleepwear and pose a risk of burn injuries.

    Product
    Children's Two-Piece Pajamas and Lounge Dresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24182·2024-04-04

    Thule RideAlong Rear-Mounted Child Bike Seats Recalled for Chemical Hazard

    Thule is recalling about 8,640 RideAlong rear-mounted child bike seats because the harness padding can contain DecaBDE, a flame retardant, in excess of regulatory limits. DecaBDE can be toxic if ingested or if it contacts skin or eyes.

    Product
    Thule RideAlong rear-mounted Child Bike Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1326-2024·2024-04-03

    Catheter Extension Recalled by Fresenius Due to Chemical Leachables

    Fresenius is recalling 479,978 stay-safe Luer Lock Catheter Extensions due to chemical leachables in the tubing. Healthcare providers should contact the manufacturer for replacement information.

    Product
    stay-safe /Luer Lock Catheter Ext. 18 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1286-2024·2024-04-03

    Nimbus II Infusion Pump Systems Recalled for Multiple Potential Device Failures

    InfuTronix is recalling 52,328 Nimbus II Infusion Pump Systems due to potential failure modes including battery failure, system errors, drug product leakage, flow rate issues, and housing damage. The devices will no longer be available or supported after June 20, 2024.

    Product
    Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1323-2024·2024-04-03

    Catheter Extension Tubing Recalled Due to Identified Leachable Substances

    Fresenius Medical Care is recalling 114,982 stay-safe Safe Lock Catheter Extensions due to peroxide cross-linked tubing leachables. Patients and healthcare providers are advised to discontinue use and contact the manufacturer for replacement.

    Product
    stay-safe /Safe Lock Catheter Ext. 12 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V248000·2024-04-03

    Aston Martin Recalls 2021 DBX Vehicles for Loose Driveline Fasteners

    Aston Martin is recalling 2021 DBX vehicles because loose fasteners on the front propeller shaft and differential may cause loss of front wheel drive or engine stall.

    Product
    ASTON MARTIN — ASTON MARTIN DBX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1327-2024·2024-04-03

    FDA Recalls Fresenius Catheter Extension Tubing Due to Chemical Leachables

    Fresenius Medical Care is recalling 105,700 stay-safe /Luer Catheter Extension 6 in devices nationwide due to chemical leachables identified in the peroxide cross-linked tubing. FDA classified this as a Class I recall.

    Product
    stay-safe /Luer Catheter Ext. 6 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1285-2024·2024-04-03

    Nimbus Ambulatory Infusion Pump recalled due to multiple failure modes

    InfuTronix is recalling Nimbus Infusion Pump Systems (Nimbus Flex, Nimbus PainPro) due to potential battery failure, system errors, drug leakage, flow rate abnormalities, and housing damage. About 52,328 units are affected nationwide.

    Product
    Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); Catalog Number IT1025. Ambulatory Infusion Pump and components
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0429-2024·2024-04-03

    Treprostinil Injection recalled nationwide due to particulate matter contamination

    Par Pharmaceutical is recalling Treprostinil Injection nationwide due to the presence of particulate matter. This FDA Class I recall affects 466 vials of lot 57014 distributed throughout the United States.

    Product
    Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-206-01
    Category
    Drug
    Distribution
    Distributed nationwide