The Recall Desk

State

Arizona product recalls

73,576 recalls have nationwide distribution and so reach Arizona. 8,391 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total
8,391
Critical
1,313
Severe
2,047
Most recent
2026-10-21

Of the 8,391 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 8,391 recalls whose distribution notice names Arizona specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

526–550 of 81967

  • SevereFDA (Devices)·Z-3150-2026·2026-09-23

    Abiomed Recalls Impella Optical Controllers Due to Purge Sensor Defect

    Abiomed is recalling Impella Optical Controllers because a purge flag component may fail, causing recognition issues. The recall covers 4,100 units distributed in the US and internationally.

    Product
    Impella Optical Controller, Automated Impella Controller, Impella Connect Package with the below product descriptions and corresponding Product Codes. 1. Optical, AIC, Impella Connect, Packaged, AU; Product Code: 0042-0040-AU. 2. Optical, AIC, Impella Connect, Packaged, CA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3195-2026·2026-09-23

    Howmedica Recalls Aged Orthopaedic Implant Components Due to Wear Risk

    Howmedica is recalling 12,156 orthopaedic implant components made with aged polyethylene material. The aging may cause excessive wear, leading to device failure and potential need for revision surgery.

    Product
    AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3204-2026·2026-09-23

    Howmedica Recalls Trident Polyethylene Knee Inserts Due to Material Aging

    Howmedica Osteonics Corp. is recalling Trident polyethylene knee inserts because aged raw material may cause excessive wear and device failure.

    Product
    TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manufactured from UHMWPE (polyethylene)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3124-2026·2026-09-23

    Medline Convenience Kits Recalled for Fungal Contamination Risk

    Medline is recalling 10,407 convenience kits containing sterile applicators that may be contaminated with Aspergillus penicillioides, posing a risk of serious infection.

    Product
    Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Number: ACC010374A; 3) ACC010679, Catalog Number: ACC010679; 4) ACC010726A, Catalog Number: ACC010726A; 5) DYNDB3061, Catalog Number: DYNDB3061; 6) DYNDH1245, Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1336-2026·2026-09-23

    Foods Alive Organic Moringa Leaf Powder Recalled for Salmonella Risk

    Foods Alive Inc. is recalling 1,691 pouches of organic moringa leaf powder due to potential Salmonella contamination. The product was sold nationwide in the US and UAE.

    Product
    Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3108-2026·2026-09-23

    AVID Medical Recalls Halyard IV Start Kits Due to Mold Contamination

    AVID Medical is recalling Halyard IV Start Kits because they contain applicators contaminated with Aspergillus penicillioides.

    Product
    Halyard IV START KIT NON-STERILE REF: KRIV26-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3130-2026·2026-09-23

    Nova Biomedical StatStrip Glucose Meter Recalled for Data Error

    Nova Biomedical is recalling StatStrip Glucose meters due to a software defect that may assign patient test results to the wrong medical record.

    Product
    StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3149-2026·2026-09-23

    Abiomed Recalls Impella Optical Controllers Due to Purge Flag Component Failure

    Abiomed is recalling 1,422 Impella Optical Controllers because a purge flag component may fail, causing purge cassette recognition issues.

    Product
    Impella Optical Controller with the below product descriptions and corresponding Product Codes. 1. Impella Optical Controller, Packaged, AU; Product Code: 0042-0010-AU. 2. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU. 3. Impella Optical Controller…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2984-2026·2026-09-23

    Bard Access Systems Recalls Power-Trialysis Dialysis Catheters

    Bard Access Systems is recalling Power-Trialysis dialysis catheters as a downstream action to a Class I recall.

    Product
    Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605240; Power-Trialysis Short-Term Straight Dialysis Catheter, REF…
    Category
    Medical Device
    Distribution
    50 states
  • HighNHTSA·26V608000·2026-09-23

    Forest River Recalls 2025-2026 Cedar Creek Trailers Due to Door Blockage

    Forest River is recalling 2025-2026 Cedar Creek fifth wheel trailers because a sleeper sofa may block the bunkroom door, potentially delaying emergency exits.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3207-2026·2026-09-23

    Medline Anesthesia Pain Kits Recalled for Potential Sterility Compromise

    Medline Industries is recalling 341 anesthesia pain kits due to open sterile seals that may compromise sterility and lead to patient infection.

    Product
    Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3200-2026·2026-09-23

    Howmedica Recalls Orthopaedic Implants Due to Potential UHMWPE Oxidation

    Howmedica is recalling specific orthopaedic implant components made with aged UHMWPE material that may oxidize, potentially leading to increased wear and device failure.

    Product
    DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-800 C-M062-7-500 C-M063-2-600 SELF-PRESSURIZING GLENOID SIZE 9 C-M063-5-000 SHOULDER - GLENOID #11 5361-6111 SHOULDER - GLENOID #5 5361-6105 SHOULDER…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3156-2026·2026-09-23

    ICU Medical Recalls Plum Administration Sets Due to Drip Chamber Discoloration

    ICU Medical is recalling Plum administration sets because drip chambers may contain black specks or discolored PVC material. The presence of particulate matter in the fluid path has not been ruled out.

    Product
    Plum administration sets
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3192-2026·2026-09-23

    Datex-Ohmeda Et Control Software Recalled for Anesthetic Delivery Interruption

    Datex-Ohmeda is recalling 410 Et Control software units for anesthesia gas machines that may interrupt anesthetic delivery, requiring clinician intervention to prevent decreased patient effect.

    Product
    Et Control, Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents, Field replaceable unit (FRU) part numbers: 1011-8000-000-S, 5700665
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3146-2026·2026-09-23

    Maquet Percutaneous Insertion Kit Recalled for Sterile Barrier Integrity Issues

    Maquet is recalling Percutaneous Insertion Kits because the packaging may not consistently maintain sterile barrier integrity, posing a risk of infection.

    Product
    Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3208-2026·2026-09-23

    Medline Recalls Minor Pack Convenience Kits Due to Open Sterile Seals

    Medline Industries is recalling 459 units of Minor Pack convenience kits because open sterile seals may compromise sterility and lead to patient infection.

    Product
    Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3137-2026·2026-09-23

    Medline Open Heart A Pack Kits Recalled for Sterility Concerns

    Medline is recalling 135 Open Heart A Pack kits in California due to a potential sterile barrier breach in the RCSP cannulae, posing a risk of infection.

    Product
    Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3175-2026·2026-09-23

    Happiest Baby SNOO Sleep Sack Recall for FDA Review Status

    Happiest Baby, Inc is recalling 1,055 units of SNOO Sleep Sacks because Extra Small and Extra Large sizes have not been reviewed for safety and effectiveness by the FDA.

    Product
    Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101 S2107-110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3198-2026·2026-09-23

    Howmedica Recalls Triathlon Hinge Inserts Due to Material Aging

    Howmedica is recalling Triathlon hinge inserts made with aged polyethylene that may wear excessively, potentially causing device fracture or the need for revision surgery.

    Product
    TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4 13MM 5612-P-413 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3164-2026·2026-09-23

    Nuclein DASH Rapid PCR Instrument Recalled for Software Issue

    Nuclein LLC is recalling 182 DASH Rapid PCR Instruments due to a software issue. The recall affects units distributed in 18 US states.

    Product
    Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software Version: 6.0.2, 6.0.4, 6.0.5, 6.0.6 Product Description: The DASH¿ Rapid PCR Instrument (DASH Instrument) is an automated, fluorescence-based…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3170-2026·2026-09-23

    GE Healthcare Recalls Workflow Core Services V8 Due to Data Association Errors

    GE Healthcare is recalling Workflow Core Services V8 because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.

    Product
    Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applications, All versions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3171-2026·2026-09-23

    GE Healthcare Recalls Core Services Hub V8 Due to Data Association Errors

    GE Healthcare is recalling Core Services Hub V8 software because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.

    Product
    Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise imaging workflows, All versions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3176-2026·2026-09-23

    Happiest Baby SNOO Sleep Sacks Recalled for Lack of FDA Review

    Happiest Baby, Inc. is recalling SNOO Sleep Sacks because they have not been reviewed for safety and effectiveness by the FDA.

    Product
    Happiest Baby, Inc. SNOO Sleep Sack, X-Large Model/Catalog Number: S2101-501 S2101-508-11 S2101-508-3 S2101-508-4 S2101-508-5 S2101-508-6 S2101-508-7 S2101-512 S2101-513 S2101-532 S2101-533 S2101-534 S2101-535 S2101-536 S2101-541 S2101-551 S2102-508-10 S2102-508-9 S2103-501…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3193-2026·2026-09-23

    Mirion Captus 4000e Thyroid Uptake System Recalled for Spring Arm Failure

    Mirion Technologies is recalling 783 Captus 4000e Thyroid Uptake Systems because a tension bolt may fail, causing the spring arm to fall unexpectedly.

    Product
    Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;
    Category
    Medical Device
    Distribution
    Distributed nationwide