State

Arizona product recalls

73,376 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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20351–20375 of 81763

HighFDA (Devices)·Z-1764-2022·2022-09-28
FDA expands recall: HLS Set Advanced 7.0 sterility barrier compromise
Maquet Medical Systems USA has expanded a recall for HLS Set Advanced 7.0, a preconnected medical device used for heart and lung support, due to a potential breach in the sterility barrier that could compromise product sterility.
Product
BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70105.2794. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2022·2022-09-28
Serological Test Positive Control Shows False Negative Results for Hepatitis B
Randox Serology I Positive Control may test negative for Hepatitis B surface antigen (HBsAg) on certain analyzers despite being designed as a positive control, potentially affecting laboratory quality control procedures.
Product
The Randox Serology I Positive Control contains the following analytes in human based plasma: Anti HIV 1/2, Anti HTLV 1/2, Anti HCV, HBsAg, Anti HBc, and Anti Treponema pallidum IgG. The product is delivered as a liquid in a kit of 3 identical ready-to-use vials of 5 mL each.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1769-2022·2022-09-28
Hemodialysis Water Purification Unit Recalled for Missing EMI Shielding
Fresenius is recalling 24 units of the AquaC UNO H reverse osmosis unit because internal ethernet cables lack ferrite cores, compromising electromagnetic compatibility in hemodialysis water purification systems.
Product
AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-10VA-1 Vivonic Part Number: G02000970-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1765-2022·2022-09-28
Medical device set recalled for potential sterility barrier compromise
Maquet Medical Systems USA is recalling the BEQ-HLS 5050 (HLS Set Advanced 5.0) due to a potential breach in the sterility barrier that may compromise product sterility.
Product
BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70105.2797. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1754-2022·2022-09-28
BD MaxGuard Extension Set Mislabeled with Wrong Expiration Year
BD MaxGuard Flow Controller Extension Set labels incorrectly list 2027 expiration instead of 2025. Use of expired product could compromise device integrity and create infection risk.
Product
BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS106
Category
Medical Device
Distribution
39 states
HighFDA (Devices)·Z-1759-2022·2022-09-28
BD MaxGuard Extension Set Recalled for Incorrect Expiration Year
CAREFUSION's BD MaxGuard Extension Set is being recalled because product labels incorrectly list expiration year 2027 instead of 2025. Using expired product may compromise integrity, potentially causing leaks and infection risk.
Product
BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171
Category
Medical Device
Distribution
39 states
HighNHTSA·22V721000·2022-09-28
Rolls-Royce Phantom Headlight Coating Defect Recall
BMW is recalling 2023 Rolls-Royce Phantom vehicles because headlights may lack metal coating, causing low beams to fail FMVSS 108 and increasing crash risk.
Product
ROLLS-ROYCE — ROLLS-ROYCE PHANTOM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2022·2022-09-28
BD MaxGuard Extension Set labeled with incorrect expiration year 2027
46,900 BD MaxGuard Extension Sets are labeled with expiration year 2027 but should expire in 2025. Using expired product may compromise integrity and cause leaks, risking infection.
Product
BD MaxGuard Extension Set with 4-way stopcock, REF: M4058
Category
Medical Device
Distribution
39 states
HighFDA (Devices)·Z-1776-2022·2022-09-28
FDA Recalls Grappler Suture Anchors Due to Potential Breakage Risk
Paragon 28, Inc. is recalling Grappler Suture Anchors (REF: P44-110-3010-SK, Lot 5007499) due to risk that the anchor may break upon insertion, potentially leaving debris in patients and delaying surgery.
Product
Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1767-2022·2022-09-28
Medical Device Recall: CARDIOHELP HLS Set Advanced Sterility Barrier Breach
Maquet Medical Systems is expanding its recall of the CARDIOHELP HLS Set Advanced due to a potential breach in the sterility barrier that could compromise product sterility, affecting 6,871 US units and 18,670 worldwide.
Product
BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1755-2022·2022-09-28
BD MaxGuard Flow Controller Extension Set recalled for mislabeled expiration dates
CAREFUSION is recalling BD MaxGuard Flow Controller Extension Sets because product labels show expiration year 2027 instead of 2025. Using expired sets risks product integrity failure and potential patient infection.
Product
BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141
Category
Medical Device
Distribution
39 states
HighFDA (Devices)·Z-1766-2022·2022-09-28
HLS Set Advanced Sterility Breach Recall for Cardiac Support Equipment
Maquet Medical Systems USA is recalling HLS Set Advanced 5050 units due to a potential breach in the sterility barrier. The defect may result in compromised product sterility for this cardiac and respiratory support equipment.
Product
BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70106.9077. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2022·2022-09-28
Absorbable Gelatin Sponge Hemostat Recalled for Endotoxin Contamination
GELITA MEDICAL GMBH recalled 3,596 boxes of ORCA FOAM hemostats after routine testing found higher than acceptable endotoxin levels. The surgical devices were distributed across the United States.
Product
ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP, REF ORCA FOAM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1738-2022·2022-09-28
Mountain Dew Major Melon Zero 12-pack cans have incorrect sugar-content labeling
Mountain Dew Major Melon Zero 12-pack cans sold nationwide are labeled 'Full Sugar' on the can despite containing Zero Sugar formula. The actual product is correct; only the can label is mislabeled.
Product
Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as 12 pack. Bottled under the authority of Pepsico, Inc. Purchase, NY 10577. UPC 0 12000 20506 4 (can) UPC 0 12000 20507 1 (12 pack carton)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1770-2022·2022-09-28
Dialysis water-treatment unit recalled for missing ferrite cores in cables
Fresenius is recalling 6 units of the AquaC UNO H reverse osmosis unit used with hemodialysis systems due to missing ferrite cores in internal ethernet cables affecting electromagnetic compatibility.
Product
AquaC UNO H [120V, 60Hz, 1700VA, US-Version- a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-0970-1 Vivonic Part Number: G02000966-US
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1774-2022·2022-09-28
Fungitell STAT IVD Assay affected by incorrect printed reconstitution instructions
Associates of Cape Cod is recalling Fungitell STAT IVD Assay kits due to incorrect printed information on clamshells regarding reconstitution and pretreatment volumes. Users should verify procedures against official documentation before use.
Product
Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Ref: FT007
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1771-2022·2022-09-28
Diversatek M-Catch Retrieval Nets: incorrect inner polybag labeling
Diversatek Healthcare is recalling M-Catch Retrieval Nets (Part Number REF 1175-01, Lot Number 001919) due to incorrect inner polybag labeling. 245 devices were distributed nationwide between September and October 2021.
Product
Diversatek Health, M-Catch Retrieval Nets, Part Number REF 1175-01, Quantity 5 EA/u. Used to endoscopically retrieve severed polyps, tissue samples, food bolus, and foreign bodies in the gastrointestinal tract.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1541-2022·2022-09-28
Clonidine Hydrochloride 0.3 mg Tablets Recalled for Strength Mix-up
UNICHEM PHARMACEUTICALS is recalling Clonidine Hydrochloride Tablets labeled 0.3 mg that contain 0.2 mg tablets instead. The recall affects 18,960 bottles (Lot # GCLH22005) distributed nationwide.
Product
CLONIDINE HYDROCHLORIDE — CLONIDINE HYDROCHLORIDE (CLONIDINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22E082000·2022-09-27
Manchester Tank Recalls Propane Tanks Due to Valve Thread Depth Defect
Manchester Tank & Equipment Co is recalling ManTank Propane Tanks because valve thread depth is less than spec, creating a risk of propane leaks and fire.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E081000·2022-09-27
Haldex Air Disc Brake Pads Recalled for Loose Retaining Clip
Haldex is recalling certain ModulT Gen II Air Disc Brakes because a loose retaining clip may detach, creating a road hazard and increasing crash risk.
Product
SERVICE BRAKES, AIR:DISC:PADS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V720000·2022-09-27
Lightning eMotors Recalls 2022 FE4 and FT3 for Brake Warning Light Defect
Lightning eMotors is recalling 2022 FE4 and FT3 vehicles because the instrument panel may fail to display brake and ABS warning lights, increasing crash risk.
Product
LIGHTNING EMOTORS — LIGHTNING EMOTORS FE4, FT3
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V719000·2022-09-26
Seagrave Recalls 2022 Emergency Vehicles Due to Tie Rod Clamp Defect
Seagrave is recalling 2022 Marauder and Capitol emergency vehicles because improperly heat-treated tie rod clamps may fail, causing a loss of steering.
Product
SEAGRAVE — SEAGRAVE CAPITAL, MARAUDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V718000·2022-09-26
2023 Volkswagen Atlas Models Recalled for Brake Line Leaks
Volkswagen is recalling 2023 Atlas and Atlas Cross Sport models due to brake lines that may leak at threaded connections. A brake fluid leak can increase stopping distance, raising crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V717000·2022-09-26
Doosan Recalls 2021-2022 Portable Air Compressors Due to Brake Seal Leak
Doosan is recalling 2021-2022 Portable Air Compressors because wheel bearing seals may leak grease into drum brakes, reducing braking performance and increasing crash risk.
Product
DOOSAN — DOOSAN PORTABLE AIR COMPRESSOR
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·034-2022·2022-09-24
Behrmann Meat and Processing Inc. Recalling Ready-to-Eat Meat Products Due to Listeria Contamination
Behrmann Meat and Processing Inc. is recalling approximately 87,382 pounds of ready-to-eat meat products because tests detected possible Listeria monocytogenes contamination. No confirmed cases of illness have been reported since the September 24, 2022 recall announcement.
Product
Behrmann Meat & Processing, Inc. — Behrmann Meat and Processing Inc. Recalls Various Ready-to-Eat Meat Products Due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide