State

Arizona product recalls

73,096 recalls have nationwide distribution and so reach Arizona. 8,385 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total: 8,385
Critical: 1,313
Severe: 1,719
Most recent: 2026-09-23

Of the 8,385 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 1,719 (21%) are Severe.

Which agencies issued them

These figures cover only the 8,385 recalls whose distribution notice names Arizona specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10676–10700 of 81481

HighFDA (Devices)·Z-2684-2024·2024-08-28
VITROS XT Chemistry Slides Recalled for Dust Contamination of Diagnostic Results
Ortho-Clinical Diagnostics is recalling 88,253 units of VITROS XT Chemistry ALB-TP Slides because they shed dust and debris during normal operation, potentially contaminating sodium test results and causing misdiagnosis.
Product
The VITROS XT Chemistry Products ALB-TP Slides is a single device that contains both an albumin test and a total protein test side by side separated by a plastic barrier sealed within a single slide frame. In this format, individual reactions occur, and test results are generated
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2582-2024·2024-08-28
Spectrum Wireless Battery Modules fail to auto-document infusion status
Spectrum Wireless Battery Modules may fail to send infusion status updates to hospital electronic medical records. The issue affects 17,377 units nationwide used with Spectrum V8 and IQ infusion pumps.
Product
Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion pump) and 3570009 (Spectrum IQ infusion pump)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2681-2024·2024-08-28
Alinity hq Analyzer May Generate Incorrect Blood Test Results
Abbott's Alinity hq Analyzer has been recalled due to software issues that can produce incorrect blood cell counts and hemoglobin measurements in certain circumstances. No illnesses have been reported.
Product
Alinity hq Analyzer, REF: 09P68-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2648-2024·2024-08-28
Alcon ophthalmic surgical knives recalled for blade sharpness defects
Alcon is recalling specific ophthalmic surgical knives (ClearCut and A-OK models) from its Custom Pak system due to blade sharpness complaints affecting 384,851 units distributed nationwide and internationally.
Product
Product Name: Alcon Custom Pak Model/Catalog Number: Many Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience kits intended for use by trained ophthalmic surgeons in a variety of ophthalmic surgeries
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2685-2024·2024-08-28
Regard Kit Decanters Recalled for Defective Sterile Packaging
ROi CPS LLC is recalling 78 Regard Kits containing Microtek decanters due to pin holes and tears in sterile packaging that cannot be identified visually. Defective packaging could compromise the sterile barrier.
Product
Regard Kit containing the Microtek decanter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0639-2024·2024-08-28
Rubbing Alcohol Recalled for Non-Sterile Water in Manufacturing
ZEE Company's 70% isopropyl rubbing alcohol is being recalled because non-sterile water was used in production instead of sterile water, violating manufacturing standards. The product was distributed nationwide in the US and Canada.
Product
Rubbing Alcohol (70% Isopropyl Alcohol), First-Aid Antiseptic, packaged in a) 3.78L (1-gallon jug); and b) 208.19L (55-gallon drum), Sold by: ZEE Company- A Member of the Vincit Group, 3401 Cummings Road, Chattanooga, TN 37419, Made in USA.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2664-2024·2024-08-28
Ophthalmic knife sharpness defect recalled for increased complaints
Alcon recalls 3,419 ophthalmic knives due to increased complaints about blade sharpness. The Class II recall affects the ClearCut SB INTREPID 2.2 ANG and related models distributed nationwide and internationally.
Product
Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number: 8065992561 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2643-2024·2024-08-28
Transfer Device REF 2008S Sterile Barrier Packaging Defect Recall
Microtek Medical's Transfer Device REF 2008S is being recalled due to pin holes and tears in the sterile packaging barrier identified during testing. These defects compromise sterility and could allow contamination.
Product
Transfer Device, REF 2008S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2649-2024·2024-08-28
Alcon ClearCut S Ophthalmic Knives Recalled for Sharpness Complaints
Alcon is recalling ClearCut S and A-OK ophthalmic surgical knives due to increased complaint reports about sharpness. Approximately 5,039 units were distributed nationwide and internationally.
Product
Product Desc: Product Name: ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2683-2024·2024-08-28
FDA Recalls BioFire Pneumonia Diagnostic Test Kits for Control Failures
BioFire Diagnostics recalls BIOFIRE FILMARRAY Pneumonia Panel plus test kits due to manufacturing defects that could lead to control failures and delayed test results. The affected kits were distributed in multiple US states and countries worldwide.
Product
BIOFIRE FILMARRAY Pneumonia Panel plus, REF: RFIT-ASY-0143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0636-2024·2024-08-28
Lidocaine HCl Injection Recall Due to Lack of Sterility Assurance
Fagron Compounding Services is recalling Lidocaine HCl Injection due to lack of assurance of sterility. Four lot numbers distributed nationwide are affected with expiration date 10/14/2024.
Product
Lidocaine HCl Injection, 2% (20mg per mL) (100 mg per 5 mL) per syringe, Rx only, Fagron Sterile Services, 8710 E. 34th St, N. Wichita, KS 57226.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0640-2024·2024-08-28
HAND-I-SAN Hand Sanitizer Recalled for Manufacturing Process Deviation
HAND-I-SAN No-Rinse Hand Sanitizer is being recalled due to manufacturing process deviations involving the use of non-sterile water in production. The product was distributed nationwide and to Canada.
Product
HAND-I-SAN, No-Rinse Hand Sanitizer (75% Isopropyl Alcohol), packaged in a) 3.78L (1-gallon jug packaged in a case of 4x1 gallon jugs), b) 18.92L (5-gallon pail), c) 208.19L (55-gallon drum), and d) 1040.98L (275-gallon tote), ZEE Company 3401 Cummings Road, Chattanooga, TN, 374
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0642-2024·2024-08-28
FDA recalls Timolol Maleate eye drops due to defective bottle cap
FDC Limited recalls Timolol Maleate Ophthalmic Solution nationwide because the bottle cap spike becomes lodged in the nozzle, preventing patients from dispensing the medication. No illnesses have been reported.
Product
TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2708-2024·2024-08-28
Medline Medical Procedure Kits Recalled for Dimensional Variation in Canister Fitting
Medline Industries is recalling 75,098 medical procedure kits due to slight dimensional variations that may cause difficulty fitting into their outer canisters. No injuries or illnesses have been reported.
Product
Medline medical procedure kits labeled as follows: a) AAA CDS, REF CDS984011C; b) CAN KIT, REF DYKM1184; c) DENTAL CDS, REF CDS984010B; d) EGD KIT, REF DYK1253578F; e) EGD REG KIT, REF DYKE1830; f) ENDO KIT, REF DYKE1516A; g) ERCP REG KIT, REF DYKM2127; h) GI P
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2687-2024·2024-08-28
Dental Digital Analog Products Recalled for Out-of-Specification Rotation
Preat Corp is recalling 185 dental digital analog products due to out-of-specification rotation affecting inspection accuracy. The devices are used in dental laboratories for visual inspection of abutments and restorations.
Product
Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-compatible WN Digital Analog, REF 9001303 3i Certain-compatible 5.0mm Digital Analog, REF 9001903 3i Certain-compatible 6.0mm Digital Analog,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2704-2024·2024-08-28
Medline Medical Procedure Kits Recalled for Canister Fitting Issues
Medline is recalling 22,891 medical procedure kits because of a slight dimensional variation that may cause difficulty fitting into the outer canister.
Product
Medline medical procedure kits labeled as follows: a) CYSTO, REF DYNJ905000D; b) ENDO KIT, REF DYKE1462A; c) ENDOSCOPY KIT, REF DYKE1431B; d) ENDOSCOPY KIT, REF DYKE1623B; e) GENERAL LAPAROSCOPY, REF DYNJ902385I; f) GENERAL LAPAROSCOPY, REF DYNJ905508G; g) GENERAL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2696-2024·2024-08-28
Medline Soft Liner Dimensional Variation May Affect Outer Canister Fit
Medline Industries is recalling 1500ML soft liners due to dimensional variations that may make fitting into the outer canister more difficult. No injuries have been reported.
Product
1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2713-2024·2024-08-28
Medline Medical Procedure Kits Recalled for Dimensional Variation Affecting Outer Canister Fit
Medline Industries is recalling certain C-Section surgical kits due to dimensional variations that could cause difficulty fitting into the outer canister. The recall affects 1,753 units distributed worldwide.
Product
Medline medical procedure kits labeled as follows: a) C-SECTION CDS, REF CDS983998C
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2709-2024·2024-08-28
Medline medical procedure kits recalled due to dimensional variation
Medline Industries is recalling 1,700 medical procedure kits due to a dimensional variation that may cause fitting difficulty into the outer canister. The affected kits were distributed in the US and internationally.
Product
Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM2169
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2694-2024·2024-08-28
Medline Soft Suction Canister Liner Recalled for Dimensional Variation
Medline Industries recalls soft suction canister liners due to dimensional variation that may cause difficulty fitting the product into the outer canister. The issue affects units distributed worldwide.
Product
LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2639-2024·2024-08-28
C-Flow Bag Decanter Packaging Defects Prompt Sterile Barrier Recall
Microtek Medical Inc. recalls C-Flow Bag Decanters (10,366 cases) due to pin holes and tears in sterile barrier packaging discovered during quality testing. The defects could allow bacterial contamination.
Product
C-Flow Bag Decanter, REF 2000S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2700-2024·2024-08-28
Medline Anesthesia Circuit Kits Recalled for Dimensional Variation
Medline is recalling three models of anesthesia circuit kits due to slight dimensional variations that may cause difficulty fitting into the outer canister. The recall affects 1920 units distributed worldwide.
Product
Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT ADULT, REF DYNJAAF6666B; b) ANESTHESIA CIRCUIT PEDS-LF, REF DYNJAP9918A; c) CV ANESTHESIA - ROOM SET UP, REF DYNJ905503F
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2702-2024·2024-08-28
Medline Dental Procedure Kits Recalled Due to Dimensional Variation
Medline Industries is recalling certain dental procedure kits due to dimensional variations that may cause difficulty fitting into the outer canister. The recall affects 99 units distributed worldwide.
Product
Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2710-2024·2024-08-28
Medline Procedure Kits Recalled Due to Dimensional Fitting Issues
Medline is recalling 160 medical procedure kits due to a dimensional variation that may make them difficult to fit into their outer canister. No injuries have been reported.
Product
Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2699-2024·2024-08-28
Medical Device Liner Recalled for Dimensional Variation Affecting Fit
Medline Industries has recalled 316,125 units of its MED-SOFT Single Liner with Solidifier due to a dimensional variation that may cause difficulty when inserting the product into the outer canister.
Product
1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PG
Category
Medical Device
Distribution
Distributed nationwide