The Recall Desk

State

Arizona product recalls

73,388 recalls have nationwide distribution and so reach Arizona. 8,387 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,387
Critical
1,313
Severe
2,047
Most recent
2026-10-02

Of the 8,387 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 2,047 (24%) are Severe.

Which agencies issued them

These figures cover only the 8,387 recalls whose distribution notice names Arizona specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22951–22975 of 81775

  • ModerateFDA (Devices)·Z-0833-2022·2022-04-06

    CareFusion Endoscopic Equipment Recalled for Missing Instructions for Use

    CareFusion endoscopic equipment packages did not contain required instructions for use. The recall affects 152 units distributed to healthcare facilities in the US and internationally.

    Product
    (a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 5 mm, 30 degrees 7", 17.5 cm, Catalog #88-5920; (c) CareFusion Snowden-Pencer MIS, Endoplastic Fitting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0831-2022·2022-04-06

    Baxter Healthcare MiniCap Extended Life PD Transfer Sets Recalled for Regulatory Non-Compliance

    Baxter Healthcare is recalling 498 units of MiniCap Extended Life PD Transfer Sets because they were distributed without FDA regulatory clearance. Affected units were distributed in 16 U.S. states.

    Product
    MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S, R5C4482, R5C4483, R5C4484
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0846-2022·2022-04-06

    BALLARD Multi-Access Port Catheter Distributed With Incorrect Expiration Dates

    Avanos Medical is recalling BALLARD Multi-Access Port Catheters because they were distributed with incorrect expiration dates on the packaging. The recall includes 6,280 devices.

    Product
    BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0738-2022·2022-04-06

    Lansoprazole Delayed-Release Capsules Recalled for Failed Dissolution Specifications

    Dr. Reddy's Laboratories is recalling 7,703 bottles of Lansoprazole Delayed-Release Capsules (30 mg, 90-count) nationwide due to failed dissolution specifications found during long-term stability testing.

    Product
    LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0837-2022·2022-04-06

    Regard Custom Procedure Kits with BD Luer Lok Access Devices Recalled

    ROi CPS LLC is recalling 1,750 Regard Custom Procedure Kits containing BD Luer Lok Access Devices distributed nationwide in Missouri.

    Product
    Regard Custom Procedure Kits containing BD Luer Lok Access Devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0828-2022·2022-04-06

    Cobas Liat respiratory virus analyzer units recalled for false Influenza B results

    Roche is recalling 14 Cobas Liat analyzer units due to detector noise causing false positive Influenza B results. Affected units were distributed in seven U.S. states and three countries.

    Product
    cobas LiatSystem, respiratory virus panel nucleic acid assay system, Material Number 07341920190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0845-2022·2022-04-06

    BALLARD Seal Cassette Replacement catheters recalled for incorrect expiration date

    Avanos Medical is recalling BALLARD Seal Cassette Replacement MAP catheter devices due to incorrect expiration dates on product labels. Affected lot 30143745 was distributed in the United States and internationally.

    Product
    BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Cassette Replacement for Multi-Access Port (MAP) Catheter; Sterile; Single Use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0838-2022·2022-04-06

    Surgical Gloves Recalled Due to Missed FDA Border Inspection

    Ansell is recalling Gammex Non-Latex PI Green surgical gloves (size 7 1/2) because the product was not submitted for required FDA inspection at the border. Distribution included Arizona, California, Nevada, Texas, Utah, and Washington.

    Product
    Gammex Non-Latex PI Green PI-KARE Skin-friendly PI Technology polyisoprene surgical gloves 7 1/2
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0726-2022·2022-04-06

    Prescription Atorvastatin Calcium Tablets Recalled for Failed Quality Specifications

    Dr. Reddy's Laboratories is recalling 28,068 bottles of Atorvastatin Calcium 80 mg tablets nationwide due to failed impurity and degradation specifications. No illnesses or injuries have been reported.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V219000·2022-04-05

    Land Rover Recalls 2016-2017 Range Rovers for Seat Belt Defect

    Jaguar Land Rover is recalling 2016-2017 Range Rover and Range Rover Sport vehicles because the driver's seat belt retractor may not lock during hard braking.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V216000·2022-04-01

    2021-2022 Autocar XPEDITOR vehicles recalled for ABS wiring defect

    Autocar is recalling 2021-2022 XPEDITOR vehicles because the ABS modulation valve may be wired incorrectly, potentially extending braking distance and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V215000·2022-04-01

    Mercedes-Maybach S 580 Recalled for Front Seat Trim Detachment Risk

    Mercedes-Benz is recalling 2021-2022 Maybach S 580 vehicles because front seat trim parts may detach during rear air bag deployment, potentially causing improper air bag function and injury.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH S 580, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E029000·2022-03-31

    GM Recalls Truck Hero Tonneau Covers for Detachment Risk

    General Motors is recalling specific Truck Hero tonneau covers for 2019-2022 Chevrolet and GMC trucks because they may detach while driving, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V210000·2022-03-31

    Chevrolet Traverse roof rail air bag harness connector defect

    General Motors is recalling certain 2020-2022 Chevrolet Traverse and 2021-2022 Buick Enclave vehicles because the harness connector to the roof rail air bags may have incompatible electrical terminals that could prevent air bag deployment in a crash.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V212000·2022-03-31

    Jayco Recalls 2022 White Hawk Travel Trailers Due to Fire Risk

    Jayco is recalling 2022 White Hawk travel trailers because loose power inlet wiring may cause an electrical arc or short, increasing the risk of a fire.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22737·2022-03-31

    SOUNDBOKS Gen. 3 Bluetooth Speakers Recalled for Battery Fire Hazard

    SOUNDBOKS Inc. is recalling about 6,700 Gen. 3 Bluetooth speakers because the removable lithium-ion battery can overheat and pose a fire hazard. Consumers should stop using the speakers immediately and contact the company for a free replacement battery.

    Product
    SOUNDBOKS (Gen. 3) Bluetooth Speakers with Lithium-Ion Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V208000·2022-03-31

    2022 Keystone Alpine Travel Trailers Recalled for Electrical Fire Risk

    Keystone is recalling 2022 Alpine and related travel trailers due to power inlet lug bolts manufactured too hard to tighten properly, causing loose electrical connections that could lead to fire.

    Product
    KEYSTONE — KEYSTONE ALPINE, AVALANCHE, PASSPORT, IMPACT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22109·2022-03-31

    Helix Metal Lockable Drug Chests Recalled Due to Locking Mechanism Failure

    Maped Helix USA is recalling about 7,700 Helix Metal Lockable Drug Chests because the locking mechanism can fail, allowing unauthorized access to medications and posing a risk of poisoning.

    Product
    Helix Metal Lockable Drug Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V209000·2022-03-31

    Keystone Cougar travel trailers recalled for outrigger tire clearance defect

    Keystone is recalling 2019-2022 Cougar travel trailers due to improper outrigger clearance that may allow tires to contact the outrigger. Damaged tires can fail and cause loss of vehicle control and increased crash risk.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22110·2022-03-31

    PlayMonster Kid O Hudson Glow Rattles Recalled for Choking Hazard

    PlayMonster is recalling Kid O Hudson Glow Rattles because the rattle's legs can break off, posing a choking hazard to young children. The firm has received three reports of legs breaking off, though no injuries have been reported.

    Product
    Kid O Hudson® Glow Rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22111·2022-03-31

    Universal Security Instruments 2-in-1 Smoke and Carbon Monoxide Alarms Recalled for Failure to Alert

    Universal Security Instruments is recalling about 8,000 combination smoke and carbon monoxide alarms that may fail to alert consumers to dangerous carbon monoxide levels. Two units have been reported to fail the alarm function, though no injuries have been reported.

    Product
    2-in-1 Photoelectric Smoke & Fire + Carbon Monoxide Alarms
    Category
    Consumer Product
    Distribution
    Distributed nationwide