The Recall Desk

State

Arizona product recalls

73,381 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 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21351–21375 of 81768

  • HighFDA (Drugs)·D-1255-2022·2022-07-27

    HYDROmorphone Injection Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center recalled 22,805 pre-filled syringes of HYDROmorphone HCl Injection due to lack of sterility assurance. Six lot numbers were distributed nationwide.

    Product
    HYDROmorphone HCl Injection, USP, 10 mg/50 mL (0.2 mg/mL) syringes, 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th Street Extension, West Columbia SC 29172, NDC: 69374-529-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1457-2022·2022-07-27

    Dark chocolate truffles recalled for undeclared tree nut allergens

    Queen Bee Gardens is recalling Dark Mint Classic Truffles for undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Products were distributed to retail locations in CO, NM, WY and nationwide online.

    Product
    Dark Mint Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11035 1. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, dry milk, whey, agar, algin, lecithin & peppermint oil. Decoration: "Ivory" chocolate & artificial color.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1471-2022·2022-07-27

    Honey Caramels Almond Coconut Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Almond Coconut due to potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Consumers allergic to tree nuts should not consume this product.

    Product
    Honey Caramels Almond Coconut. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz bag: 788394 12004 6. Ingredients: Honey, butter (pasteurized cream & salt), cream, almonds, coconut, nonfat dry milk, whey, natural flavors, lecithin…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1424-2022·2022-07-27

    Randox Cholesterol In Vitro Diagnostic Kits Fail Stated Performance Specifications

    Randox Cholesterol diagnostic kits fail to meet stated performance specifications. Calibration issues cause quality control results to fall outside acceptable ranges, potentially delaying test results.

    Product
    Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1487-2022·2022-07-27

    Chocolate Cashew Candy Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honeymoons Ivory Chocolate Cashew candy because it may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts, which can cause severe allergic reactions.

    Product
    Honeymoons Ivory Chocolate Cashew. PLU Code: 788394 14900 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1461-2022·2022-07-27

    Queen Bee Gardens Huckleberry Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Huckleberry Truffles because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide via internet.

    Product
    Huckleberry Truffle. Net wt. 1.4 oz. PLU Code: 788394 11057 3. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], HONEY, "Ivory" chocolate (sugar, cocoa butter, whole & non-fat milk solids, sunflower…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1264-2022·2022-07-27

    Lidocaine HCl injection syringes recalled due to sterility assurance failure

    Nephron Sterile Compounding Center has recalled 37,310 syringes of Lidocaine HCl Injection USP 1% nationwide due to lack of assurance of sterility. Affected lots expire between August and October 2022.

    Product
    Lidocaine HCl Injection, USP 1%, 50 mg/5 mL (10 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-985-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1464-2022·2022-07-27

    Bee Energy Bar recalled due to undeclared tree nuts

    Queen Bee Gardens is recalling Bee Energy Bars due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.

    Product
    Bee Energy Bar. Net wt. 1.5 oz. PLU Code: 788394 18559 5. Ingredients: Dark chocolate (sugar, chocolate liquor, cocoa butter, milk fat [butter], sunflower lecithin, pure vanilla), honey, almonds, butter (pasteurized cream, salt), coconut, gluten free oats, dried…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1282-2022·2022-07-27

    Aspirin-Dipyridamole Capsules Recalled for Capsule Breakage Defect

    Glenmark Pharmaceuticals is recalling Aspirin and Extended-Release Dipyridamole Capsules due to capsule breakage defects. Approximately 168,936 bottles were distributed nationwide.

    Product
    ASPRIN AND EXTENDED-RELEASE DIPYRIDAMOLE — ASPRIN AND EXTENDED-RELEASE DIPYRIDAMOLE (ASPRIN AND EXTENDED-RELEASE DIPYRIDAMOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1386-2022·2022-07-27

    Stryker Trevo Trak 21 Microcatheter recalled for missing carton product illustration

    Stryker Neurovascular is recalling 71 Trevo Trak 21 Microcatheter units because the product carton label is missing the required product drawing or illustration.

    Product
    Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413; TREVO NXT 4X41+TRAK21 2-PACK - CE, REF: 91414; TREVO NXT 6X37+TRAK21 2-PACK - CE, REF: 91415; TREVO NXT 4X28+TRAK21+CAT6 3-PACK - CE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1422-2022·2022-07-27

    Laboratory Reagent Recalled Due to Inaccurate Calibration Curves

    Randox Laboratories is recalling Soluble Transferrin Receptor reagent (TF10159) due to calibration curve defects causing inaccurate test results on Siemens Atellica CH analyzers.

    Product
    Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1423-2022·2022-07-27

    Soluble Transferrin Receptor Calibrator Recall Due to Lab Errors

    Randox Laboratories is recalling Soluble Transferrin Receptors Calibrator kits used in lab analyzers. The calibrators can produce incorrect test results, with some values potentially underestimated by up to 30 percent.

    Product
    Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1340-2022·2022-07-27

    FDA Recalls Launch Sequence Euphoria Capsules as Unapproved Drug

    Launch Sequence Euphoria Capsules were marketed without FDA approval. Consumers should discontinue use immediately and contact the manufacturer.

    Product
    Launch Sequence Euphoria Capsules, 10- count tins, ASIN B08ZJX4V9J, UPC Code 661020846864.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1244-2022·2022-07-27

    OTC Hydrogen Peroxide Solution Recalled for Isopropyl Alcohol Contamination

    Vi-Jon's hydrogen peroxide topical solution has been recalled due to cross-contamination with low levels of isopropyl alcohol. Multiple brands are affected nationwide in the USA and Canada.

    Product
    HYDROGEN PEROXIDE — HYDROGEN PEROXIDE (HYDROGEN PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1394-2022·2022-07-27

    Triton Sponge System Software Instructions Updated for Proper Sponge Handling

    Stryker is updating the Instructions for Use for the Triton Sponge System software (versions 4.6.5, 4.8.7, 4.9.6) to clarify proper handling technique for sponges and calibration placard. The FDA Class III recall affects 51 units distributed nationwide.

    Product
    Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1390-2022·2022-07-27

    Erythropoietin Control Product Instructions Contain Incorrect CE Marking

    R & D Systems is replacing Instructions for Use (IFU) for Quantikine IVD Erythropoietin Human Serum Controls due to an incorrect CE marking designation that should not appear on the self-certified product.

    Product
    Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human serum and plasma. IFU, Part Number 750095
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V539000·2022-07-26

    Spartan Fire Recalls 2020-2021 Metrostar and Gladiator Trucks for Fire Risk

    Spartan Fire is recalling 2020-2021 Metrostar and Gladiator fire trucks because a loose electrical connection may cause the load center to overheat and increase the risk of a fire.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V537000·2022-07-26

    Capacity Recalls 2021-2022 TJ Trucks for Steering Gear Fracture Risk

    Capacity of Texas is recalling 2021-2022 TJ 5000, 6500, and 9000 trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.

    Product
    CAPACITY — CAPACITY TJ 9000, TJ 6500, TJ 5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V538000·2022-07-26

    E-One Fire Trucks Recalled for Electrical Connection Overheating Risk

    E-One is recalling specific 2019-2022 fire trucks because a loose electrical connection may cause the load center to overheat, increasing fire risk.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON, TYPHOON N, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V536000·2022-07-26

    Ferrari Recalls Multiple Models Due to Brake Fluid Reservoir Cap Defect

    Ferrari is recalling various models from 2005-2022 because a defective brake fluid reservoir cap may cause a leak, leading to partial or total loss of brake function.

    Product
    FERRARI — FERRARI LAFERRARI, LAFERRARI APERTA, 612 SCAGLIETTI, F12 BERLINETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V529000·2022-07-22

    Ember Recalls 2022 Overland Trailers Due to LP Gas Leak Risk

    Ember is recalling 2022 Overland series trailers because cracked LP gas fittings may cause a leak, increasing the risk of fire.

    Product
    EMBER — EMBER OVERLAND SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V531000·2022-07-22

    Spartan RV Chassis Steering Gear Assembly Defect Recall

    Shyft Group is recalling certain 2022-2023 Spartan RV Chassis vehicles due to improperly assembled steering gears that may fracture, causing loss of steering control. Owners should contact the manufacturer for free inspection and replacement.

    Product
    SPARTAN — SPARTAN K4, K2, K3, K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V528000·2022-07-22

    2022 Ford F-53 Steering Wheel Attachment Bolt May Loosen

    Ford is recalling certain 2022 F-53 and F-59 motorhome and commercial chassis vehicles because the steering wheel attachment bolt may loosen and separate. This could result in loss of steering control and increased crash risk.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V532000·2022-07-22

    Thomas Built Buses Minotour Recalled for Incorrect Tire Labeling

    Daimler Trucks North America is recalling 2019-2023 Thomas Built Buses Minotour school buses because tire labels list the wrong size, potentially affecting vehicle stability.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR SRW
    Category
    Vehicle
    Distribution
    Distributed nationwide