The Recall Desk

State

Arizona product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21601–21625 of 81775

  • SevereFDA (Food)·F-1370-2022·2022-07-06

    Fudge Trio Holiday Fudge Tray Recalled Nationwide for Salmonella Contamination

    Fudgeamentals LLC is recalling Marketside and Walmart Fudge Trio Holiday Fudge Trays nationwide due to Salmonella contamination in the peanut butter ingredient. Consumers should discard these products and not consume them.

    Product
    1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. 2. WALMART MKT FUDGE TRIO (6-16 OZ) HOLIDAY FUDGE TRAY FUDGEAMENTALS
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V464000·2022-07-06

    Cummins Recalls 2020-2022 Trailer-Mounted Generator Sets Due to Shutdown Defect

    Cummins is recalling 2020-2022 C500D6Re trailer-mounted generator sets because a logic error may prevent them from shutting down, posing burn and shock risks.

    Product
    CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1298-2022·2022-07-06

    TEG5000 Analyzer displays incorrect PlateletMapping assay results in TEG Manager

    Haemonetics' TEG5000 Analyzer displays incorrect PlateletMapping assay values when connected to TEG Manager Software versions 1.1–4.3.1, potentially affecting laboratory test interpretation.

    Product
    Product Name: TEG5000 Analyzer (07-022, 07-033) with TEG Analytical Software (07-030, 07-031) and TEG Platelet Mapping Assay - PlateletMapping ADP & AA (07-014), PlateletMapping ADP (07-015), PlateletMapping AA (07-016). Issue occurs when Platelet Mapping Assay results…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1172-2022·2022-07-06

    Fluticasone Propionate Nasal Spray Recalled Due to Defective Container

    Akorn, Inc. is recalling 44,400 bottles of Fluticasone Propionate Nasal Spray nationwide due to a defective container that prevents proper dispensing. Patients should contact their healthcare provider or pharmacist.

    Product
    Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1385-2022·2022-07-06

    Wilton Rainbow Chip Crunch Sprinkles recalled due to milk contamination

    Wilton Industries is recalling Rainbow Chip Crunch Sprinkles (5.25 oz) due to milk contamination. The recall affects 6,400 units distributed nationwide and internationally.

    Product
    Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 710-5364
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1300-2022·2022-07-06

    Orthopedic Plates Recalled Due to Incorrect Etching and Mislabeling

    One lot of DVR Anatomic distal radius orthopedic plates was incorrectly etched during manufacturing and may have been placed into kits labeled as a different plate model. The affected plates were distributed to healthcare facilities nationwide.

    Product
    DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and osteotomies involving the distal radius.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22E054000·2022-07-06

    Cummins Recalls PD7000 Electric Drivetrains Due to Electrical Grounding Defect

    Cummins is recalling PD7000 Electric Drivetrains because an improperly grounded air compressor can cause electric shock. Owners will receive a free repair to install a ground strap.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1285-2022·2022-07-06

    Backup batteries in Avance CS2 anesthesia machines fail prematurely

    GE Healthcare is recalling backup batteries in Avance CS2 and CS2 Pro anesthesia machines manufactured after April 1, 2019. Batteries may fail earlier than expected, affecting approximately 6,600 devices worldwide.

    Product
    Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1309-2022·2022-07-06

    GCX Channel Mounting Accessory Screws May Loosen or Pull Out

    Skytron recalls its GCX Channel Mounting Accessory (model H8-300-40-A) because mounting screws may loosen or pull out when used as a monitor mount on surgical booms. Affected units were distributed worldwide.

    Product
    Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1169-2022·2022-07-06

    Methylphenidate Patch Recall: Defective Delivery System and Adhesive Issues

    Daytrana (methylphenidate) patches are being recalled due to ripping patches and poor adhesive transfer affecting drug delivery. This Class II recall involves 8,559 cartons distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1162-2022·2022-07-06

    Losartan Potassium tablets recalled for elevated AZIDO impurity

    PD-Rx Pharmaceuticals recalled Losartan Potassium 50 mg tablets nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits. The recall affects 687 bottles across multiple lots.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1304-2022·2022-07-06

    HydroSurg Plus Laparoscopic Irrigator recalled for inability to irrigate

    Davol HydroSurg Plus Laparoscopic Irrigators cannot provide irrigation. The FDA issued a Class II recall affecting 4,780 units worldwide.

    Product
    HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, with Cojoined Suction and Irrigation Tubing, Catalog number 0026880
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1295-2022·2022-07-06

    CV Minor Kit with Nonsterile Component Recalled for Contamination Risk

    ROi CPS LLC is recalling 180 CV Minor Kit units due to a nonsterile component accidentally packaged in the sterile kit, posing a contamination and infection risk.

    Product
    regard Item Number: 800774001, CV00979A - CV Minor Kit, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1284-2022·2022-07-06

    Tacrolimus Calibrator Set Recalled for Inaccurate Immunoassay Quantitation

    The QMS Tacrolimus Calibrator Set is recalled because calibrators recovered 82-94% of target values, causing inaccurate (over-quantitated) patient drug test results. This affects healthcare facilities in 20 US states and 9 countries.

    Product
    QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3 QMS TACROLIMUS CAL C 10015568-3 QMS TACROLIMUS CAL D 10015569-3 QMS TACROLIMUS CAL E 10015570-3 QMS TACROLIMUS CAL F 10015571-3
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-1292-2022·2022-07-06

    Medical Device App Records Inaccurate Urinary Flow When Hearing Aids Active

    The ProudP Everyday Uroflow Tracker app may record lower-than-actual urination measurements when a hearing aid or AirPods Live Listen feature is active on the same iPhone, due to interference with the app's sound-based measurement system.

    Product
    ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1290-2022·2022-07-06

    Central venous catheter recalled for incorrect gravity flow rates

    Arrow International is recalling the Arrow Three-Lumen CVC due to incorrect gravity flow rates on the product lidstock. The defect may affect fluid and medication delivery through the catheter.

    Product
    Arrow Three-Lumen CVC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1161-2022·2022-07-06

    Losartan Potassium Tablets Recalled for Manufacturing Impurity Issues

    PD-Rx Pharmaceuticals recalls Losartan Potassium Tablets (25 mg, 90-tablet bottles) due to Current Good Manufacturing Practice deviations. Specific lot numbers contain AZIDO impurity levels above acceptable limits.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1163-2022·2022-07-06

    Losartan Potassium Tablets Recalled for Elevated AZIDO Impurity Levels

    PD-Rx Pharmaceuticals is recalling Losartan Potassium 100 mg tablets due to AZIDO impurity levels above acceptable limits detected during manufacturing. Approximately 1,320 bottles were distributed nationwide.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V476000·2022-07-06

    2021–2022 Cargo trailers recalled for defective safety chains

    Forest River is recalling certain 2021–2022 Cargo Mate and Continental Cargo Trailers because safety chains don't meet weight rating specifications. A chain failure could cause the trailer to detach from the tow vehicle, increasing crash risk.

    Product
    CONTINENTAL CARGO — CONTINENTAL CARGO, CARGO MATE CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1287-2022·2022-07-06

    Medline Pill Splitters recalled for unhinged lid exposing sharp blade

    Medline is recalling over 840,000 pill splitters due to a defect where the product lid can come unhinged, exposing a sharp blade and posing a laceration risk.

    Product
    Medline Pill Splitters; 1 each/box; 144 boxes/carton
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1296-2022·2022-07-06

    SOLTIVE SuperPulsed Laser Fibers recalled for model and size labeling mismatch

    Olympus is recalling certain SOLTIVE SuperPulsed Laser Fibers because device model and size may be mismatched between packaging and the actual device. This could result in the wrong laser fiber being used in medical procedures.

    Product
    SOLTIVE SuperPulsed Laser Fibers, Model# Labeled TFL-FBX150BS (Carton) - 150 Micron Ball Tip Single Use Fiber Model # Labeled TFL-FBX200S (Pouch) - 200 Micron Single Use Fiber Model # Labeled TFL-FBX200BS (Carton) - 200 Micron Ball Tip Single Use Fiber Model # Labeled…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1294-2022·2022-07-06

    Artis Pheno fluoroscopic system may lose video display signals

    Siemens Artis Pheno fluoroscopic X-ray systems may lose video signals from the Large Display during procedures. In rare cases, both transceivers could fail, affecting displays in the examination and control rooms.

    Product
    Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1297-2022·2022-07-06

    Atrium Firm PVC Thoracic Catheter Recall Due to Expiration Date Mismatch

    Atrium Medical Corporation is recalling Atrium Firm PVC Thoracic Catheter 28French due to an expiration date mismatch between the sterile barrier pouch and case labels. The discrepancy allowed product to be used up to five days past its true expiration date.

    Product
    Atrium Firm PVC Thoracic Catheter 28French-Intended to facilitate the evacuation of air and/or fluid from the chest cavity or mediastinum. Product REF Number: 15028
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Drugs)·D-1164-2022·2022-07-06

    FDA Recalls Losartan-Hydrochlorothiazide Tablets for Manufacturing Quality Deviations

    Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets (100 mg/25 mg) due to CGMP deviations and azido impurity levels exceeding acceptable limits. The affected lot is BLM2114A (expiration 07/2023) distributed nationwide.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide