State

Arizona product recalls

73,218 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 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16851–16875 of 81605

HighFDA (Devices)·Z-1691-2023·2023-06-14
Sterile Surgical Procedure Packs Recalled for Defective Light Handle Covers
DeRoyal Industries is recalling 2,972 sterile surgical procedure packs containing light handle covers that have been recalled by another manufacturer. The affected packs were distributed to hospitals in Virginia.
Product
Sterile custom surgical procedure packs: (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital; (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital; (3) 89-10509.02, LAPAROTOMY PACK, Stonewall Jackson Hospital; (4) 89-10517.04, CNRV BASIC SETUP PACK, New River…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1689-2023·2023-06-14
TREO Abdominal Stent-Graft Label Does Not Match Actual Device Size
Bolton Medical is recalling the TREO Abdominal Stent-Graft System because the carton label may not match the actual stent-graft size inside. Implanting the wrong size stent-graft could result in surgical complications.
Product
The TREO ABDOMINAL STENT-GRAFT SYSTEM (TREO) consists of four types of implants, specifically a Main Bifurcated Stent-Graft, a Leg Extension Stent-Graft, a Proximal Cuff Stent-Graft and a Straight Iliac Extension Stent-Graft. Each stent-graft is preloaded into its own delivery…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0865-2023·2023-06-14
Empower Pharmacy Ascorbic Acid Injection Mislabeled as Preserved
Empower Pharmacy is recalling Ascorbic Acid 500 mg/mL injection solution because vials labeled as preserved are actually preservative-free. The 504 affected vials were distributed nationwide.
Product
ASCORBIC ACID PRESERVED INJECTION SOLUTION, 500 mg/mL, 30 mL Sterile Multiple-Dose Vial, RX ONLY, Compounded by: Empower Pharmacy, 5980 W Sam Houston Pkwy N Ste 300 Houston, TX 77041, NDC 72627-2405-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1682-2023·2023-06-14
BD Veritor System Instructions for Use Not FDA Approved
The Instructions for Use for BD Veritor System rapid diagnostic tests for COVID-19 and flu were not FDA-approved, lacking proper specimen type specifications. Using the test with invalid specimen types could produce false positive or negative results, potentially delaying diagnosis or treatment.
Product
BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B, 30 Single Use Test Devices- Intended for the in vitro, simultaneous qualitative detection and differentiation of SARS-CoV-2 nucleocapsid antigen and influenza A and/or B Catalog Number: 256088
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1686-2023·2023-06-14
SMMT ambIT Kit Basic Filter Luer Cass Recalled for Missing In-Line Filter
Avanos Medical recalls SMMT ambIT Kit Basic Filter Luer Cass units that were distributed without the required air in-line filter component.
Product
SMMT ambIT Kit Basic Filter Luer Cass, Product Code: 220537
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1692-2023·2023-06-14
Surgical Procedure Packs Recalled Due to Included Light Handle Covers
DeRoyal Industries is recalling two models of custom surgical procedure packs because they contain light handle covers that were previously recalled by another manufacturer. The packs were distributed in Virginia.
Product
Sterile custom surgical procedure packs (1) 89-10529.04, CNRV OR C-SECTION PACK, New River Valley Medical Center; and (2) 89-10567.05, OB-OR C-SECTION PACK, Carilion Roanoke Memorial Hospital.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0870-2023·2023-06-14
Glycopyrrolate Injection Vials Recalled Due to Labeling Mix-up
HF Acquisition Co LLC is recalling Glycopyrrolate Injection 0.2mg/mL due to a label mix-up affecting specific lots distributed in Texas, Arizona, and California.
Product
GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
Category
Drug
Distribution
3 states
ModerateFDA (Devices)·Z-1694-2023·2023-06-14
ESR Diagnostic Quality Control Material Incorrectly Labeled as Different Level
RR Mechatronics Starrsed Control Level N ESR vials were mislabeled as a different control level, causing instruments to flag results as out of range. The mislabeling affects approximately 9,306 units worldwide.
Product
RR Mechatronics Starrsed Control Level N ESR Control 4.6 ml QRR049001- In-vitro diagnostic quality control material to monitor the precision of Starrsed Erythrocyte Sedimentation Rate (ESR) instruments and procedures. Product Code: A0026577
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0869-2023·2023-06-14
Buprenorphine Sublingual Tablets Recalled for Manufacturing Quality Deviations
Sun Pharmaceutical recalls 12,336 bottles of Buprenorphine 8 mg sublingual tablets (Lot DND1515A) due to Good Manufacturing Practice deviations identified during manufacturing.
Product
BUPRENORPHINE — BUPRENORPHINE (BUPRENORPHINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1695-2023·2023-06-14
ESR Diagnostic Control Vials Recalled for Incorrect Lot Labeling
Mechatronics USA recalls approximately 10,752 units of ESR quality control vials due to incorrect lot labeling that causes instrument results to be falsely flagged as out of range.
Product
RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro diagnostic quality control material to monitor the precision of Starrsed Erythrocyte Sedimentation Rate (ESR) instruments and procedures. Product Code: A0026578
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1696-2023·2023-06-14
Abbott Alinity i Anti-TPO Reagent Kit Recalled for Fill Volume Error
Abbott is recalling Alinity i Anti-TPO Reagent Kit (Lot 46009FN00) due to a manufacturing error resulting in marginally lower fill volume than specified in the Instructions for Use. Approximately 110 kits were distributed nationwide across 17 US states.
Product
Alinity i Anti-TPO Reagent Kit, List Number 09P3521
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V424000·2023-06-13
Blue Bird Recalls 2022-2024 All American Transit Buses for Brake Warning Defect
Blue Bird is recalling 2022-2024 All American transit buses because a software error may prevent air pressure gauges and low air warnings from functioning, increasing crash risk.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V425000·2023-06-13
Blue Bird Recalls School Buses Due to Air Brake Warning Failure
Blue Bird is recalling 2021-2024 All American and 2021-2022 Vision school buses because a software error may prevent air pressure warnings from functioning, increasing crash risk.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V423000·2023-06-13
Peterbilt 579 trucks recalled for electrical fire risk from fastener defect
PACCAR is recalling 2021-2023 Peterbilt 579 trucks with MX-13 engines because an improperly installed fastener can chafe the alternator cable, increasing fire risk.
Product
PETERBILT — PETERBILT 579
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V422000·2023-06-13
Tesla Recalls 2023 Semi Trucks for Door Warning System Defect
Tesla is recalling 2023 Semi trucks because the door warning system allows drivers to dismiss alerts about unlatched doors, increasing injury risk.
Product
TESLA — TESLA SEMI
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V421000·2023-06-12
2022 Nissan Sentra: Driver Cowl Seal Defect May Cause Electrical Failures
The 2022 Nissan Sentra may have a defective driver's side cowl seal, allowing water intrusion and electrical corrosion. This could cause loss of airbag function, exterior lighting, and braking safety features, increasing crash and fire risk.
Product
NISSAN — NISSAN SENTRA
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·022-2023·2023-06-09
J.T.M. Provisions Recalls Homestyle Chili Topping for Undeclared Soy Allergen
J.T.M. Provisions is recalling approximately 200 pounds of ready-to-eat Homestyle Chili Topping because it may contain beef taco filling with undeclared soy.
Product
J.T.M. Provisions Company — J.T.M. Provisions Company Recalls Ready-To-Eat Homestyle Chili Topping Product Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighNHTSA·23E044000·2023-06-09
East Penn Recalls Deka 648MF Batteries Due to Electrical Spark Risk
East Penn is recalling Deka 648MF batteries because an incomplete electrical connection may cause sparks, increasing the risk of injury.
Product
ELECTRICAL SYSTEM:12V/24V/48V BATTERY recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V418000·2023-06-09
Ford Recalls 2022-2023 F-150 Lightning Due to Rear Lightbar Defect
Ford is recalling 2022-2023 F-150 Lightning vehicles because microcracks in the rear lightbar lens can cause reverse lights to fail or flicker.
Product
FORD — FORD F-150 LIGHTNING BEV
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23E045000·2023-06-09
SAF-Holland Recalls Suspension Systems Due to Tire Pressure Loss Risk
SAF-Holland is recalling CBXA40 and ULX40 suspension systems with Tire Pilot Plus management systems because all eight tires may lose pressure at speeds over 45 mph.
Product
TIRES:PRESSURE MONITORING AND REGULATING SYSTEMS recall
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·23V420000·2023-06-09
Ford vehicles recalled for missing head restraint adjustment instructions
Ford recalls 2018-2023 Expedition, Navigator, and F-Series vehicles lacking head restraint adjustment instructions. Improper adjustment increases crash injury risk.
Product
FORD — FORD, LINCOLN F-350 SD, F-250 SD, F-450 SD, F-550 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V411000·2023-06-08
Chrysler Recalls Jeep and Ram Vehicles for Engine Stall Risk
Chrysler is recalling 2014-2020 Jeep Grand Cherokee and 2014-2019 Ram 1500 vehicles with 3.0L Diesel engines because a sensor defect may cause the engine to stall, increasing crash risk.
Product
JEEP — JEEP, RAM GRAND CHEROKEE, 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V413000·2023-06-08
Jeep Grand Cherokee Models Recalled for Detaching Rear Coil Springs
Chrysler is recalling certain 2022-2023 Jeep Grand Cherokee and 2021-2023 Jeep Grand Cherokee L vehicles. Rear coil springs may detach while driving, creating a crash risk; dealers will repair them free.
Product
JEEP — JEEP GRAND CHEROKEE 4XE, GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V416000·2023-06-08
Autocar Recalls 2022-2023 Legend Vehicles Due to Steering Column Weld Defect
Autocar is recalling 2022-2023 Legend vehicles because the steering column shaft may not be properly welded, which could cause a loss of steering control.
Product
AUTOCAR — AUTOCAR LEGEND
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V417000·2023-06-08
Altec Recalls 2022-2023 TG-124S Trailers Due to Loose Axle U-Bolts
Altec is recalling 2022-2023 TG-124S trailers because axle U-bolts may loosen and detach, increasing crash risk. Owners should contact Altec for a free inspection and tightening.
Product
ALTEC — ALTEC TG-124S
Category
Vehicle
Distribution
Distributed nationwide