State

Arizona product recalls

72,986 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.

Which agencies issued them

These figures cover only the 8,381 recalls whose distribution notice names Arizona specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7826–7850 of 81367

CriticalFDA (Food)·F-0588-2025·2025-03-12
Watermelon and Cucumber Products Recalled for Potential Salmonella Contamination
JFE Franchising is recalling watermelon and cucumber products with Tajin seasoning due to potential Salmonella contamination. Affected packages were distributed in TX, LA, WY, and AZ with sell-by dates from October 12 through December 5, 2024.
Product
Mixed Melon, Cucumber & Tajin 18 oz Watermelon & Cucumber w/ Tajin 18 oz packed in clamshells
Category
Food
Distribution
4 states
CriticalFDA (Devices)·Z-1257-2025·2025-03-12
Insulin pump recall: Medtronic Paradigm models malfunction during airplane flight
Medtronic MiniMed's Paradigm insulin pumps can malfunction during airplane flight due to air pressure changes, potentially causing dangerously high or low blood sugar levels that could be fatal.
Product
Paradigm insulin pump, REF: MMT-754
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1244-2025·2025-03-12
Rotarex Atherectomy Catheter Recalled for Helix Fracture Risk
Bard is recalling Rotarex Atherectomy System catheters due to potential helix fracture or breakage that could cause vessel injury and severe bleeding. Updated instructions are being distributed to clarify procedural steps to reduce this risk.
Product
Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0606-2025·2025-03-12
Amazon Fresh Jumbo Sugar Cookies recalled for undeclared egg allergen
Amazon Retail LLC is recalling Amazon Fresh Jumbo Sugar Cookies nationwide due to undeclared egg, a major allergen. Consumers with egg allergies should not consume the affected cookies.
Product
ASIN B084PZ7K98, Amazon Fresh Jumbo Sugar Cookie, 27 oz (12 count), product is baked and packaged in flexible plastic bag. 4-day shelf life. UPC 465712007998. ASIN B084PX9V31, Amazon Fresh Jumbo Sugar Cookie, 2.3 oz (1 count), product is baked and sold from open pastry tray in s
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0586-2025·2025-03-12
Cucumber Products Recalled Due to Potential Salmonella Contamination
JFE Franchising Inc. is recalling packaged cucumber products distributed in TX, LA, WY, and AZ due to potential Salmonella contamination. Consumers should not consume these products.
Product
Cucumber, Lime & Tajin 19 oz Cucumber with Ranch 9 oz Cucumber Bowl with Ranch 15 oz Cucumber Slices with Tajin 15 oz packed in clamshells
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1246-2025·2025-03-12
Medtronic Pipeline Vantage device recall: deformation may cause blood clots
The Pipeline Vantage Embolization Device may malfunction, with the braid deforming or not positioning correctly, potentially causing blood clots. Approximately 7,820 units are affected worldwide.
Product
Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3-021-250-14, PED3-021-350-20, PED3-021-250-20, PED3-021-300-16, PED3-021-300-20, PED3-021-275-12, PED3-021-275-16, PED3-021-325-12, PED3-021-325-14, PED3-021-325-16, PED3-021-325-20,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1263-2025·2025-03-12
Insulin Pump Recalled for Abnormal Delivery During Flight Pressure Changes
Medtronic MiniMed 720G insulin pumps may malfunction during airplane travel due to air pressure changes, causing abnormal insulin doses that can lead to severe low or high blood sugar emergencies.
Product
MiniMed insulin pump, REF: 720G (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1254-2025·2025-03-12
Baxter Spectrum IQ Infusion System may have missing motor mounting screws
Baxter Spectrum IQ Infusion Systems may lack motor mounting screws due to a servicing defect. The FDA Class I recall affects 323 units distributed nationwide.
Product
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1245-2025·2025-03-12
Medtronic Pipeline Vantage Embolization Device Recall for Structural Deformation Risk
Medtronic is recalling approximately 18,245 unused Pipeline Vantage embolization devices due to incomplete wall apposition and braid deformation that may lead to thrombosis and serious adverse events.
Product
Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14, PED3-027-350-16, PED3-027-350-20, PED3-027-350-25, PED3-027-400-12, PED3-027-400-14, PED3-027-400-16, PED3-027-400-18, PED3-027-400-20, PED3-027-400-25, PED3-027-400-30,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0590-2025·2025-03-12
Chef Salad Recall: Potential Salmonella Contamination in Clamshells
JFE Franchising Inc is recalling approximately 1,950 packages of 11 oz Chef Salad due to potential Salmonella contamination. The affected products were distributed in Texas, Louisiana, Wyoming, and Arizona with sell-by dates from October 12, 2024, through December 5, 2024.
Product
Chef Salad 11 oz packed in clamshells
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1253-2025·2025-03-12
Baxter Sigma Spectrum Infusion System Recalled for Missing Mounting Screws
Baxter Healthcare is recalling 66 units of Sigma Spectrum Infusion System (V6) due to potential missing motor mounting screws that may have occurred during servicing. Missing screws could affect the device's operation.
Product
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0589-2025·2025-03-12
Cobb Salad Products Recalled for Potential Salmonella Contamination
JFE FRANCHISING INC is recalling Cobb Salad products (22 oz and 11 oz packages) due to potential Salmonella contamination. Products were distributed in Texas, Louisiana, Wyoming, and Arizona.
Product
Family Cobb Salad 22 oz Cobb Salad 11 oz packed in clamshells
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0585-2025·2025-03-12
Garden Salad Products Recalled for Potential Salmonella Contamination
JFE Franchising is recalling garden salad products due to potential Salmonella contamination. Products were distributed in Texas, Louisiana, Wyoming, and Arizona.
Product
Garden Salad 12 oz Family Garden Salad 24 oz packed in clamshells
Category
Food
Distribution
4 states
SevereNHTSA·25V152000·2025-03-12
Shyft Recalls 2025 Utilimaster Upfit Vehicles for Loose Seat Bolts
Shyft Group is recalling 2025 Utilimaster Upfit vehicles because passenger jump seat mounting bolts may not be properly tightened, increasing injury risk in a crash.
Product
UTILIMASTER — UTILIMASTER UPFIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V154000·2025-03-12
BMW X3 rear brake hoses may leak and disable rear braking
BMW is recalling certain 2025 X3 30 xDrive and X3 M50 xDrive vehicles because the rear brake hoses may leak, causing a loss of rear brake function, ABS and stability control.
Product
BMW — BMW X3
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0607-2025·2025-03-12
Frozen Sugar Cookie Dough Recalled for Undeclared Egg Allergen
Amazon Fresh Bake at Home Jumbo Sugar Cookie dough is being recalled due to undeclared egg. Consumers with egg allergies should not consume this product.
Product
ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Sugar Cookie 30oz, product is frozen dough, and packaged in flexible plastic bag. UPC 446472006995.
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V046000·2025-03-12
Freightliner Recalls eCascadia and eM2 Trucks for Power Loss Risk
Daimler Trucks North America is recalling 2020-2026 Freightliner eCascadia and eM2 trucks because a faulty power module may cause a loss of drive power, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER EM2, E-CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0587-2025·2025-03-12
Vegetable trays and bowls recalled for potential Salmonella contamination
JFE FRANCHISING INC is recalling vegetable bowls and trays sold in TX, LA, WY, and AZ due to potential Salmonella contamination. Consumers should not consume these products.
Product
Vegetable Bowl 13 oz Small Vegetable Tray 19.5 oz Vegetable Bowl 26 oz Large Vegetable Tray 42 oz packed in clamshells
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1293-2025·2025-03-12
Alcon Custom Pak surgical packs mislabeled as latex-free despite containing latex
Alcon surgical procedure packs contain latex but are labeled as latex-free, creating risk of allergic reaction for patients with latex sensitivity. The company is recalling 2,511 affected units.
Product
Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05, 13894-16, 17550-08, 12236-18, 11854-15, 8043-29, 12466-17, 15599-17, 14764-09, 13194-16, 17069-09
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1260-2025·2025-03-12
Medtronic MiniMed Insulin Pumps Recalled for Abnormal Delivery During Air Pressure Changes
Medtronic is recalling MiniMed insulin pumps that malfunction during airplane takeoff and landing due to air pressure changes. The defect can cause abnormal insulin delivery, leading to severe hypoglycemia, hyperglycemia, seizure, coma, or death.
Product
MiniMed insulin pump, REF: 640G (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1265-2025·2025-03-12
MiniMed Insulin Pump May Malfunction at High Altitude During Flight
Medtronic MiniMed insulin pumps may deliver abnormal insulin doses during airplane takeoff or landing due to air pressure changes, potentially causing severe low or high blood sugar.
Product
MiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0256-2025·2025-03-12
Nelarabine prescription injection recalled due to failed quality specifications
Zydus Pharmaceuticals is recalling 1,893 vials of Nelarabine Injection (250 mg/50 mL) due to failed quality specifications for impurities and degradation. Patients should contact their healthcare provider about the recall.
Product
NELARABINE — NELARABINE (NELARABINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0255-2025·2025-03-12
Prescription Nelarabine Injection Recalled for Failed Purity and Degradation Specifications
Zydus Pharmaceuticals is recalling nationwide lots of Nelarabine Injection, a cancer medication, due to failed purity and degradation specifications. The affected vials did not meet required quality standards.
Product
NELARABINE — NELARABINE (NELARABINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1256-2025·2025-03-12
Medtronic Paradigm insulin pump recall for abnormal delivery during flight
Medtronic MiniMed Paradigm insulin pumps may deliver incorrect insulin doses during airplane takeoff or landing due to air pressure changes. This can cause severe high or low blood sugar requiring immediate medical attention.
Product
Paradigm insulin pump, REF: MMT-522, MMT-523, MMT-551, MMT-722, MMT-723, MMT-751
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1262-2025·2025-03-12
Medtronic MiniMed insulin pump recalled for abnormal delivery during air pressure changes
Medtronic MiniMed insulin pumps may deliver insulin abnormally during airplane take-off or landing due to air pressure changes, risking severe low or high blood sugar emergencies.
Product
MiniMed insulin pump, REF: 700G (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
Category
Medical Device
Distribution
Distributed nationwide