State

Arizona product recalls

73,219 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: 1,720
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 1,720 (21%) are Severe.

Which agencies issued them

These figures cover only the 8,387 recalls whose distribution notice names Arizona specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17776–17800 of 81606

ModerateFDA (Drugs)·D-0528-2023·2023-04-12
Cyanocobalamin injection vials recalled for failing potency tests
Accord Healthcare recalled 4,574 cartons of Cyanocobalamin injection (Lot R2200394) nationwide after testing showed the drug was sub-potent and failed to meet strength specifications.
Product
Dodex Injectable Cyanocobalamin Injection, USP 1,000 mcg/mL, 25 x1 ML Multiple dose vials, For Intramuscular or Subcutaneous Use Only, Rx Only, Sterile, Manufactured by: Intas Pharmaceuticals Limited Pharmaz Ahnedabad 382 213, INDIA, Manufactured for: Accord Healthcare, Inc.…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0502-2023·2023-04-12
Rosuvastatin 40mg tablets recalled nationwide for manufacturing process deviations
RemedyRepack is voluntarily recalling Rosuvastatin 40mg tablets due to manufacturing practice deviations. The recall affects specific lot numbers expiring 07/31/2025 distributed nationwide.
Product
Rosuvastatin 40mg tablets, packaged in a) 45-count bottles (NDC 70518-1311-01), and b) 90-count bottles (NDC 70518-0484-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0491-2023·2023-04-12
Drug Recall: Atorvastatin 10 mg tablets due to manufacturing process violations
RemedyRepack Inc. is recalling specific lots of Atorvastatin 10 mg tablets distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations. The voluntary recall was initiated March 20, 2023.
Product
Atorvastatin 10 mg tablets, packaged in a) 30-count bottles (NDC 70518-1946-00) and b) 90-count bottles (NDC 70518-1946-01), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0490-2023·2023-04-12
Drug Recall: Aripiprazole 5mg Tablets Due to Manufacturing Practice Deviations
RemedyRepack Inc. is recalling Aripiprazole 5mg tablets (lot J0620431-052322) due to cGMP deviations affecting manufacturing practices. The voluntary recall includes 3 bottles distributed nationwide.
Product
Aripiprazole 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2921-03
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0508-2023·2023-04-12
Alprazolam 1 mg tablets recalled due to manufacturing contamination concerns
Direct Rx is recalling Alprazolam 1 mg tablets nationwide due to potential cross contamination at the manufacturer. No illnesses or injuries have been reported.
Product
Alprazolam C-IV, 1 mg, packaged in a) 30 Tabs per bottle, NDC 72189-213-30; b) 60 Tabs per bottle, NDC 72189-213-60; Rx only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0515-2023·2023-04-12
Doxazosin Tablets Recalled Due to Manufacturing Process Deviations
Preferred Pharmaceuticals is recalling Doxazosin Tablets, USP, 4 mg (lot L1522V, expiration 4/30/2025) due to current Good Manufacturing Practice deviations discovered during FDA inspection of the manufacturer, Accord Healthcare. The product was distributed nationwide.
Product
Doxazosin Tablets, USP, 4 mg, 100-count bottle, Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703, NDC 68788-7149-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0519-2023·2023-04-12
Rosuvastatin Calcium Tablets Recalled for Manufacturing Deviations
Preferred Pharmaceuticals, Inc. is recalling Rosuvastatin Calcium 10 mg tablets nationwide due to cGMP deviations identified during FDA inspection of the manufacturing facility.
Product
ROSUVASTATIN CALCIUM — ROSUVASTATIN CALCIUM (ROSUVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0514-2023·2023-04-12
Doxazosin Tablets Recalled Due to Manufacturing Practice Deviations
Preferred Pharmaceuticals recalls Doxazosin Tablets USP 2 mg (Lot H3122K, expires 5/31/2024) due to current Good Manufacturing Practice deviations identified at the manufacturing facility.
Product
Doxazosin Tablets, USP, 2 mg, 100-count bottle, Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703, NDC 68788-7328-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1320-2023·2023-04-12
Biosense Webster guiding sheath recalled for labeling mismatch
Biosense Webster is recalling 316 units of Carto Vizigo guiding sheaths because the carton label does not match the inner sterile pouch label, potentially affecting product identification.
Product
Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Medium), REF D-1385-02-S, RX CE 2797, Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0500-2023·2023-04-12
Rosuvastatin 5mg Tablets Recalled Due to Manufacturing Deviations
RemedyRepack Inc. voluntarily recalled 132 bottles of Rosuvastatin 5mg tablets nationwide due to current Good Manufacturing Practice deviations. No illnesses or injuries have been reported.
Product
Rosuvastatin 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-3519-00
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0516-2023·2023-04-12
Finasteride Tablets Recalled Due to Manufacturing Process Deviations
Preferred Pharmaceuticals is recalling specific lots of Finasteride Tablets, 5 mg due to manufacturing process deviations discovered during FDA inspection of manufacturer Accord Healthcare. No illnesses or injuries have been reported.
Product
Finasteride Tablets, USP, 5 mg, packaged in: a) 30-count bottles (NDC 68788-6976-3); b) 90-count bottles (NDC 68788-6976-9), Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Food)·F-0696-2023·2023-04-12
Shirakiku Furikake Seaweed Flakes Recalled for Incorrect Crustacean Labeling
Wismettac Asian Foods is recalling Shirakiku Furikake Seasoned Roasted Seaweed Flakes Spicy due to incorrect crustacean labeling. The company distributed 17,517 packages across 22 states.
Product
FURIKAKE SEASONED ROASTED SEAWEED FLAKES SPICY Product #38246 Brand name: Shirakiku Distributed by: Wismettac Asian Foods, Inc. 13409 Orden Drive Santa Fe Springs, CA 90670
Category
Food
Distribution
22 states
SevereNHTSA·23E031000·2023-04-11
Meritor Recalls Front Drive Steer Axles Due to Fastener Loosening
Meritor is recalling specific front drive steer axles because fasteners may loosen, potentially causing axle separation and loss of vehicle control.
Product
STEERING:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V259000·2023-04-07
Thomas Built Buses Recall 48 School Buses for Steering Defect
Daimler Trucks North America is recalling 48 Thomas Built Buses school buses because a missing fastener may allow the steer arm to detach, risking loss of steering control.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2 JOULEY, SAF-T-LINER C2, SAF-T-LINER MVP-EF, HDX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V207000·2023-04-07
Lightning eMotors Recalls 148 Vehicles Due to Battery Pack Defects
Lightning eMotors is recalling 148 electric vehicles because defective battery pack welds may cause internal leaks, leading to battery failure, loss of power, or fire.
Product
LIGHTNING EMOTORS — LIGHTNING EMOTORS FT3-86, FE4-129, FE4-86, FT3-43
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V255000·2023-04-07
Volvo VNR Trucks Recalled for Aggressive Adaptive Cruise Control Braking
Volvo Trucks is recalling 2020-2023 VNR Electric vehicles equipped with Adaptive Cruise Control that can trigger aggressive braking under light load conditions, risking rear axle skidding and loss of vehicle control.
Product
VOLVO — VOLVO VNR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V257000·2023-04-07
Buell Recalls 2021-2022 1190 RX and SX Motorcycles for Gear Shift Defect
Buell Motorcycles is recalling 2021-2022 1190 RX and SX motorcycles because an improperly installed index spring may cause gear slipping or shifting failure, increasing crash risk.
Product
BUELL — BUELL 1190 RX HAMMERHEAD, 1190 SX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V256000·2023-04-07
Alamo Group Recalls 2014-2019 Super Products Camel and Mud Dog Trailers
Alamo Group is recalling 2014-2019 Super Products Camel and Mud Dog trailers because a tie rod could disconnect, allowing the water tank strap to detach and become a road hazard.
Product
SUPER PRODUCTS — SUPER PRODUCTS CAMEL, MUD DOG
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-04072023-01·2023-04-07
Russ' Commissary Fresh Salads Recalled Due to Possible Listeria Contamination
The USDA FSIS issued a public health alert recalling fresh salads with chicken and ham containing lettuce due to possible Listeria monocytogenes contamination.
Product
Russ' Commissary — FSIS Issues Public Health Alert for Fresh Salads With Chicken and Ham Containing Lettuce Recalled by FDA for Possible Listeria Monocytogenes Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·23V254000·2023-04-07
Starcraft Prodigy School Buses Recalled for Ceiling Panel Defect
Forest River Bus is recalling 2019-2022 Starcraft Prodigy school buses because improperly secured ceiling panels may not protect passengers in a crash.
Product
STARCRAFT BUS — STARCRAFT BUS PRODIGY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V258000·2023-04-07
2023 Subaru Ascent Tire Bead Damage Increases Crash Risk
Subaru is recalling certain 2023 Ascent vehicles equipped with 20-inch wheels due to potential tire bead damage during manufacturing. The defect may cause sudden air pressure loss and increase crash risk.
Product
SUBARU — SUBARU ASCENT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V246000·2023-04-06
Prevost Recalls 2023 X3-45 VIP Motor Coaches Due to Fire Risk
Prevost is recalling 2023 X3-45 VIP motor coaches because a missing grommet allows electrical cables to chafe, potentially causing a short circuit and fire.
Product
PREVOST — PREVOST X3-45 VIP
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V250000·2023-04-06
Ducati Recalls 2023 Diavel V4 Motorcycles Due to Foot Peg Breakage
Ducati is recalling 2023 Diavel V4 motorcycles because passenger foot pegs may break, increasing the risk of a crash or injury.
Product
DUCATI — DUCATI DIAVEL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V253000·2023-04-06
2023 BMW X5 Head Restraints May Fail in Crash
BMW is recalling approximately 235 certain 2023 X5 vehicles with defective second-row head restraints that may not properly restrain occupants during a crash, violating federal safety standards.
Product
BMW — BMW X5
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23174·2023-04-06
Mammut Avalanche Shovels Recalled for Spring Locking Mechanism Failure
Mammut Sports Group is recalling Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels because the spring locking mechanism can fail during emergency excavation, posing risk of injury or death.
Product
Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels
Category
Consumer Product
Distribution
Distributed nationwide