State

Arizona product recalls

73,198 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 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15101–15125 of 81585

HighCPSC·24010·2023-10-19
Thomas & Friends Wooden Railway Troublesome Truck Toys Recalled for Choking and Magnet Ingestion
Fisher-Price is recalling about 21,000 Thomas & Friends Wooden Railway Troublesome Truck train cars because the magnetic connector piece can detach, posing choking and magnet ingestion hazards.
Product
Thomas & Friends Wooden Railway Troublesome Truck & Crates and Thomas & Friends Wooden Railway Troublesome Truck & Paint
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V709000·2023-10-19
2023 Jaguar I-PACE vehicles recalled for battery fire risk
Jaguar is recalling 2019-2023 I-PACE vehicles due to battery overheating risk from an incomplete prior repair. Owners must park and charge outside until the software update is installed and for 30 days after.
Product
JAGUAR — JAGUAR I-PACE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V701000·2023-10-19
Alliance RV fifth wheel trailers recalled for loose solar electrical connection
Alliance RV is recalling 2021-2023 Paradigm and Valor fifth wheel trailers because a wire connector in the solar panel electrical system may loosen and overheat, creating a fire risk.
Product
ALLIANCE RV — ALLIANCE RV PARADIGM, VALOR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0028-2024·2023-10-18
FDA Recalls Fresenius 2008T Hemodialysis Systems Due to PCBA Leaching
Fresenius Medical Care is recalling 703 units of the Fresenius 2008T Hemodialysis System nationwide due to potential PCBA (printed circuit board assembly) leaching from machine tubing.
Product
2008T Hemodialysis SYS, with CDX
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0034-2024·2023-10-18
Hemodialysis machines recalled due to potential circuit board material leaching
Fresenius Medical Care is recalling 733 units of 2008T hemodialysis systems nationwide due to potential leaching of printed circuit board assembly material from tubing. No illnesses or injuries have been reported.
Product
2008T HD SYS. W/O CDX BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0035-2024·2023-10-18
Hemodialysis Systems Recalled for Potential PCBA Tubing Leaching
Fresenius Medical Care is recalling 733 hemodialysis machines nationwide due to potential leaching of circuit board material from tubing. Affected equipment may contaminate blood or dialysate during treatment.
Product
2008T HD SYS. W/O CDX W/BIBAG BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0029-2024·2023-10-18
Hemodialysis machines recalled for potential printed circuit board contamination
Fresenius Medical Care is recalling 733 2008T Hemodialysis Systems without CDX due to potential PCBA leaching from tubing. This FDA Class I recall affects units distributed nationwide.
Product
2008T Hemodialysis System without CDX
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0006-2024·2023-10-18
10ML Syringe Luer Lock Recalled for Potential Blood Backfill Leakage
Fresenius Medical Care is recalling 124,773 boxes of 10ML Syringe Luer Lock syringes due to potential blood backfill leakage and foreign material contamination.
Product
10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0033-2024·2023-10-18
Hemodialysis machines recalled for potential PCBA leaching from tubing
Fresenius Medical Care is recalling 733 units of 2008T HD hemodialysis machines nationwide due to potential PCBA leaching from tubing. The FDA classified this as a Class I recall.
Product
2008T HD SYS. CDX W/BIBAG BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0031-2024·2023-10-18
Medical device manufacturer recalls hemodialysis machines for potential PCBA leaching
Fresenius Medical Care is recalling 733 units of the 2008T GEN 2 Bibag hemodialysis machine due to potential printed circuit board assembly material leaching from tubing. All affected units were distributed domestically.
Product
2008T GEN 2 Bibag without CDX
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0005-2024·2023-10-18
FDA Recalls Fresenius 10mL Luer Lock Syringes Due to Leakage and Foreign Material
Fresenius Medical Care is recalling 10mL syringes nationwide due to potential blood backfill leakage and foreign material. The recall affects 124,773 boxes of the devices.
Product
10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0042-2024·2023-10-18
FDA recalls BREXAFEMME tablets due to cross-contamination with ezetimibe
The FDA is recalling BREXAFEMME antifungal tablets due to potential cross-contamination with ezetimibe during manufacturing, with two lot numbers distributed nationwide.
Product
BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons, Rx Only, Manufactured for and distributed by SCYNEXIS, Inc., Jersey City, NJ 07302 NDC 75788-115-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0030-2024·2023-10-18
2008T Hemodialysis System recalled for potential PCBA leaching from tubing
Fresenius Medical Care is recalling 733 units of the 2008T Hemodialysis System due to potential leaching of printed circuit board material from machine tubing. Patients using affected devices should contact their healthcare provider.
Product
2008T Hemodialysis System w/Bibag
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0007-2024·2023-10-18
Syringes with Luer Lock Recalled for Blood Backfill and Foreign Material Risk
Fresenius Medical Care is recalling 3ML syringes with Luer Lock due to potential blood backfill leakage and foreign material contamination. The recall affects 124,773 boxes distributed nationwide.
Product
3ML Syringe Luer Lock with needle 20GX1, Part Number 15-03ML-0, 100 per box, 24 boxes per case
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0032-2024·2023-10-18
Hemodialysis Machines Recalled Due to Potential PCBA Leaching
Fresenius Medical Care is recalling 733 hemodialysis machines nationwide due to potential printed circuit board material leaking from tubing.
Product
2008T HD SYS. CDX BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0090-2024·2023-10-18
Cardinal Health Recalls Surgical Procedure Packs With Recalled Components
Cardinal Health is recalling 13,351 procedure packs used in surgical procedures because they contain recalled components. The affected packs were distributed nationwide and in Canada.
Product
Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0102-2024·2023-10-18
Knee Tibial Insert Recalled Due to Component Mix-Up in Packaging
Encore Medical is recalling the EMPOWR 3D Knee Tibial Insert due to a packaging error where hip and knee components were swapped, potentially causing surgeons to use the wrong implant during surgery.
Product
EMPOWR 3D Knee Tibial Insert, 5R, 10MM, VE, REF: 342-10-705
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0074-2024·2023-10-18
Flower Orthopedics Cannulated Reamer Recalled for Breaking During Surgical Use
The FDA is recalling Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer because the device can break during use, potentially requiring revision surgery.
Product
Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the intramedullary canal to the appropriate depth for nail insertion; Flex-Thread TM 3.2mm is provided sterile, single use. Catalogue Number: 8528-1-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0082-2024·2023-10-18
RoyalVibe Unapproved Medical Devices Recalled Due to Lack of FDA Authorization
RoyalVibe Health recalled multiple unapproved medical devices including ultrasound generators and therapy devices never FDA-authorized or cleared. Users could forgo legitimate medical treatment based on unproven marketing claims.
Product
CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water Restructuring Pad, RoyalVibe Therapy Balls
Category
Medical Device
Distribution
38 states
HighFDA (Devices)·Z-0076-2024·2023-10-18
Medfusion Syringe Pumps Recalled for Force Sensor Calibration Drift
The Medfusion Syringe Pump Model 3500-500 may experience force sensor calibration drift, causing false alarms or delayed occlusion detection. Approximately 20,815 units are being recalled worldwide, with increased risk in devices manufactured before April 2022.
Product
Medfusion Syringe Pump, Model 3500-500, v3, v4, v5, and v6
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V700000·2023-10-18
BMW 750e and multiple 2023-2024 models recalled for steering wheel sensor defect
BMW is recalling certain 2023-2024 models including the 750e due to a faulty ground connection in the steering wheel electrical system. The defect may render the hands-on detection system inoperative, preventing the emergency stopping assistant from engaging and increasing crash risk.
Product
BMW — BMW 740I, I5, I7, I7 M70
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0080-2024·2023-10-18
Medfusion Infusion Pump Plunger Sensor Calibration Drift Recall
Smiths Medical is recalling Medfusion infusion pump components due to a force sensor calibration issue that may cause delayed occlusion detection, false alarms, or system failures. No injuries have been reported.
Product
Medfusion PLUNGER FLOAT PLATE, Component Number G6000069, used on infusion pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0104-2024·2023-10-18
Multichem control vials break during shipping or thawing due to glass defect
TECHNO-PATH MANUFACTURING LTD. is recalling Multichem S Plus and related control vials due to a defect in the glass vial commodity. The vials may break during delivery, thawing, or opening, potentially exposing users to biohazardous material and delaying patient results.
Product
Multichem S Plus, Part Codes: a) 08P88-10, b) 08P88-11, c) 08P88-12
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23E081000·2023-10-18
Harbor Freight Recalls Kenway LED Rear Tri-Marker Bar Running Lights
Harbor Freight is recalling specific Kenway LED rear lights that may fail to illuminate due to packaging damage, increasing crash risk.
Product
EXTERIOR LIGHTING recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0077-2024·2023-10-18
Medfusion Syringe Pump Sensor Calibration Drift May Cause False Alarms
Smiths Medical is recalling Medfusion Model 3500VX-500 Syringe Pumps due to force sensor calibration drift that can cause false alarms, system failures, or delayed occlusion detection.
Product
Medfusion Syringe Pump, Model 3500VX-500, v3, v4, v5, and v6
Category
Medical Device
Distribution
Distributed nationwide