State

Arizona product recalls

73,187 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 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13726–13750 of 81574

HighFDA (Devices)·Z-0834-2024·2024-02-07
Endoscopic Surgical Stapler Reload May Fail to Form Complete Staple Line
An endoscopic surgical stapler reload may fail to properly form staples during use, potentially leaving tissue inadequately sealed. This could lead to bleeding or require additional surgery.
Product
ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SURFACE TECHNOLOGY (GST), ECHELON Endopath Stapler, Endoscopic Linear Cutter Reload (+Gripping Surface technology), 45MM WHITE VASCULAR/THIN, Product No. GST45W
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0827-2024·2024-02-07
Custom Surgical Procedure Kits Recalled for Sterilization Assessment Failures
American Contract Systems has recalled 2,717 custom surgical procedure kits used in neurosurgery nationwide. Components were added without proper assessment of their suitability for the sterilization process.
Product
Custom procedural convenience kits and trays, general hospital use, labeled as: a) IR NEURO PACK, kit number AGNE20J; b) ADULT CRANIOTOMY PACK, kit number LLCR99; c) LAMINECTOMY PACK, kit number LLLC26; d) KIT, CRANIOTOMY, kit number MMCR11J; e) KIT, NEURO SPINE, kit…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0899-2024·2024-02-07
Knee Replacement Component Recalled Due to Material Oxidation Risk
Howmedica Osteonics is recalling Scorpio NRG Tibial Brg Insert Assembly knee replacement components due to potential oxidation of raw materials over 5 years of age, which could affect material properties.
Product
Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0908
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0895-2024·2024-02-07
FDA Recalls SCORPIO U-DOME Knee Implants for Potential Material Oxidation
Howmedica is recalling SCORPIO U-DOME PATELLA knee replacement implants manufactured with UHMWPE material over 5 years old due to potential elevated oxidation levels that could affect material properties.
Product
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0797-2024·2024-02-07
Hot Sauce Recalled for Missing Wheat Allergen Labeling
Benny T's Vesta Dry Hot Sauce is recalled because its label does not list wheat and other required ingredient common names, posing a risk to consumers with wheat allergies.
Product
the original BENNY T'S VESTA DRY HOT SAUCE GHOST NET WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs (enriched flour, water, sugar, yeast, salt, non-hydrogenated vegetable shortening), Olive Oil, Salt, Natural Preservatives. UPC 7 94571 99498 0 (Habanero & Bhut…
Category
Food
Distribution
24 states
HighNHTSA·24V074000·2024-02-07
Eldorado XHF and Arrivo Recalled for Wheelchair Lift Beacon Defect
Eldorado is recalling 2012-2023 XHF and Arrivo vehicles because wheelchair lift warning beacons may be too dim, increasing injury risk.
Product
ELDORADO — ELDORADO XHF, ARRIVO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V079000·2024-02-07
Blue Bird Recalls Transit Buses Due to Incorrectly Installed Seats
Blue Bird is recalling 2021-2023 Vision and All American transit buses because convertible seats may be incorrectly installed, posing a crash injury risk.
Product
BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, ALL AMERICAN TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0867-2024·2024-02-07
Aesculap Needle Holders Distributed With Incorrect Product Labels and Packaging
Aesculap Inc. is recalling needle holder models that were distributed with incorrect product labels. The MB215R was labeled as MB362R and vice versa, which may cause procedural delays.
Product
MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND HNDLSTR203MM"
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0890-2024·2024-02-07
Knee replacement implant recalled due to material oxidation risk
Howmedica Osteonics is recalling a knee replacement patellar component that may have been manufactured with oxidized raw material. Products using UHMWPE over 5 years old can develop elevated oxidation and degraded material properties.
Product
SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-2110
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0873-2024·2024-02-07
Series II Tibial Bear Insert Recalled for Potential Material Degradation
Howmedica Osteonics Corp. is recalling the Series II Tibial Bear Insert for knee replacement because UHMWPE material over 5 years old may develop elevated oxidation that can affect the component's material properties.
Product
SERIES II TIBIAL BEAR INSERT-Intended for knee replacement Part Number: 3052-0515
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0916-2024·2024-02-07
Knee replacement tibial insert recalled due to material oxidation risk
Howmedica Osteonics Corp. is recalling DURATION knee replacement tibial inserts manufactured with raw materials over 5 years old that have developed oxidation. Oxidation can degrade the material's structural properties, affecting implant performance.
Product
DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-709
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0889-2024·2024-02-07
Total Knee Replacement Component Recalled Due to Oxidation Risk
Howmedica Osteonics Corp. is recalling SCORPIO Total Knee replacement components from specific manufacturing batches due to potential oxidation in raw materials over 5 years old. Oxidation can impact the material's properties.
Product
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-0910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0906-2024·2024-02-07
Knee replacement implant insert recalled due to material degradation risk
Howmedica Osteonics Corp. is recalling a knee replacement implant insert due to potential material oxidation. UHMWPE raw material over 5 years old may develop elevated oxidation levels, affecting implant properties.
Product
LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0823-2024·2024-02-07
Urological procedural kits recalled due to sterilization defects
American Contract Systems recalled 1,031 urological procedure kits nationwide due to sterilization process defects. Components may have damaged functionality, reduced drug efficacy, or elevated sterilization residuals.
Product
Custom procedural convenience kits and trays, urological, labeled as: a) UROLOGY DAVINCI PACK, kit number HGUR87G; b) CYSTO PACK, kit number LVCY20; c) URO ROBOTIC PACK, kit number LVUR44;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0955-2024·2024-02-07
Philips MRI Coil Seal Adhesive May Fail and Create Sharp Patient Contact Surfaces
Philips has recalled certain SmartPath to dStream MRI coil components because the seal adhesive may fail, creating sharp edges that could contact patients during scanning and cause skin and tissue injuries.
Product
SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0888-2024·2024-02-07
Knee Replacement Implant Recalled Due to Material Oxidation Risk
Howmedica Osteonics recalled Scorpio Total Knee prosthetics with UHMWPE components produced from raw material over 5 years old, which may develop elevated oxidation and affect implant properties.
Product
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-0710
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0897-2024·2024-02-07
Knee replacement component recalled due to potential material oxidation
Howmedica Osteonics recalls SCORPIO U-DOME PATELLA knee components. Older UHMWPE raw material may have elevated oxidation, potentially affecting material properties.
Product
SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0799-2024·2024-02-07
Benny T's Vesta Hot Sauce Recalled for Undeclared Wheat Allergen
Benny T's Vesta Dry Hot Sauce is recalled because wheat is not declared in the ingredient statement. The missing wheat label poses a risk to consumers with wheat allergies.
Product
the original BENNY T'S VESTA DRY HOT SAUCE REAPER NET WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs (enriched flour, water, sugar, yeast, salt, non-hydrogenated vegetable shortening), Olive Oil, Salt, Natural Preservatives. UPC 7 94571 99490 4 (Carolina Reaper)
Category
Food
Distribution
24 states
HighFDA (Devices)·Z-0951-2024·2024-02-07
Philips Ingenia 3.0T CX MRI: Loose Coil Seal May Cause Sharp Edges
Philips is recalling Ingenia 3.0T CX MRI machines due to potential failure of the Quadrature Body Coil seal adhesive. Loose seals may create sharp edges that risk skin injury or hair entanglement during scanning.
Product
Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0925-2024·2024-02-07
PS Lipped Tibial Insert Assy Duracon Knee Implant Oxidation Risk
Howmedica Osteonics is recalling PS Lipped Tibial Insert knee replacement components manufactured with aged UHMWPE material that may develop oxidation, potentially affecting device properties and performance.
Product
PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-416
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0877-2024·2024-02-07
Knee Replacement Implant Insert Recalled Due to Material Degradation Risk
Howmedica Osteonics is recalling SCORPIO TS TIB INSERT knee replacement components due to potential oxidation of raw material. Material degradation could affect implant durability.
Product
SCORPIO TS TIB INSERT-Intended for knee replacement Part Number:72-4-7512
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V078000·2024-02-07
Blue Bird Recalls School Buses Due to Improperly Installed Convertible Seats
Blue Bird is recalling 2020-2024 Vision and All American school buses because convertible seats may be incorrectly installed, creating a risk of injury during a crash.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0886-2024·2024-02-07
Knee Replacement Component Recalled Due to Raw Material Oxidation Risk
Howmedica Osteonics Corp. is recalling a SCORPIO TOTAL KNEE prosthesis component because UHMWPE raw material over 5 years old may have elevated oxidation levels affecting material properties and implant performance. Consumers with this implant should contact their physician for guidance.
Product
SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-0110
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0918-2024·2024-02-07
Knee replacement implants recalled for potential material degradation
Howmedica Osteonics Corp. is recalling DURATION Plastic Patella knee replacement implants due to potential oxidation in UHMWPE raw material over 5 years old, which may affect implant durability.
Product
DURATION PLASTIC PATELLA-DURACON Intended for knee replacement Product Number: 6642-2-200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0938-2024·2024-02-07
EZDilate Fixed Wire Balloon Medical Device Recalled Due to Device Failures
Olympus is recalling 8,294 EZDilate Fixed Wire Balloon devices due to reports of device failures including bursting, leaking, and foreign body retention in patients undergoing esophageal dilation.
Product
EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). Model: BD-400P-2080
Category
Medical Device
Distribution
Distributed nationwide