The Recall Desk

State

Arizona product recalls

73,584 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
1,311
Severe
2,049
Most recent
2026-10-21

Of the 8,391 recalls naming Arizona we have scored against our rubric, 1,311 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,049 (24%) are Severe.

Which agencies issued them

These figures cover only the 8,391 recalls whose distribution notice names Arizona specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28601–28625 of 81975

  • ModerateFDA (Devices)·Z-0807-2021·2021-01-20

    Baxter Recalls VERITAS Collagen Matrix Patches Due to Undersized Width

    Baxter Healthcare is recalling 192 units of VERITAS Collagen Matrix patches because they may have undersized width dimensions. The recall covers US and international distribution.

    Product
    VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0847-2021·2021-01-20

    Visby Medical Recalls 282 COVID-19 Test Kits for Labeling Errors

    Visby Medical is recalling 282 COVID-19 test kits because some boxes incorrectly state the product is CLIA Waived and some components expire before the kit expiration date.

    Product
    visby medical COVID-19 Test kit *** An in vitro diagnostic for the qualitative detection of SARS-CoV-2 - Product Usage: The Visby Medical COVID-19 Test is only for use under the Food and Drug Administration s Emergency Use Authorization.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0844-2021·2021-01-20

    Ortho VITROS Chemistry TP Slides Recalled for Eltrombopag Interference

    Ortho Clinical Diagnostics is recalling VITROS Chemistry TP Slides because the drug eltrombopag can interfere with total protein measurements.

    Product
    VITROS Chemistry Products TP Slides- IVD measure total protein (TP) concentration in serum and plasma using VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems Product Code: 8392292
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0860-2021·2021-01-20

    Medtronic Intellis Spinal Cord Stimulator Software Recall

    Medtronic is recalling the Intellis Spinal Cord Stimulator software due to a defect that prevents clinicians from programming the implantable neurostimulation device.

    Product
    Medtronic Intellis Spinal Cord Stimulator, Model Number A710, Clinical Programmer application version 1.3.80 - Product Usage: intended for use by clinicians in the programming of the following Medtronic neurostimulators (external and implantable) for pain therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0845-2021·2021-01-20

    Ortho Clinical Diagnostics Recalls VITROS XT Chemistry Products ALB-TP Slides

    Ortho Clinical Diagnostics is recalling VITROS XT Chemistry Products ALB-TP Slides due to potential interference from the drug eltrombopag.

    Product
    VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) - IVD quantitatively measures total protein (TP) concentration in serum and plasma using VITROS XT 3400 Chemistry Systems and VITROS XT 7600 Integrated Systems Product Code: 6844293
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0224-2021·2021-01-20

    KVK-Tech Recalls Benzhydrocodone and Acetaminophen Tablets Due to Impurity

    KVK-Tech, Inc. is recalling 528 bottles of Benzhydrocodone and Acetaminophen Tablets because the N-Oxide impurity exceeded specifications during stability testing.

    Product
    Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manufactured for: KVK-Tech, Inc., Newtown, PA 18940 USA, NDC 10702-344-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0223-2021·2021-01-20

    US Compounding Recalls Succinylcholine Chloride Injection Due to Labeling Error

    US Compounding Inc is recalling 1,534 syringes of Succinylcholine Chloride Injection because the lot number and expiration date were printed in the wrong position, making them illegible.

    Product
    Succinylcholine Chloride PF Inj. 200 mg/10 mL, 10 mL single use syringes, Rx only, US Compounding, 1270 Don's Lane, Conway, AR 72032
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·21070·2021-01-19

    Rapala Recalls Rechargeable Fillet Knives Due to Fire Hazard

    Rapala USA is recalling about 128,000 rechargeable fillet knives because the batteries can overheat and catch fire if non-Rapala chargers are used.

    Product
    Rapala® Rechargeable Fillet Knives (Item No. RRFN)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E004000·2021-01-19

    Auxbeam Headlight Bulb Recall for Excessive Glare and Brightness

    Guangzhou Zhilan E-Commerce is recalling specific Auxbeam headlight bulbs sold on Amazon that may create excessive glare for oncoming drivers, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2021·2021-01-15

    Nestlé Prepared Foods recalls pepperoni hot pockets due to possible foreign matter contamination

    The USDA Food Safety and Inspection Service is recalling approximately 762,615 pounds of not-ready-to-eat pepperoni hot pockets because they may contain glass and hard plastic fragments. One consumer reported a minor oral injury, but no additional illness cases were reported.

    Product
    Nestlé Prepared Foods Recalls Not-Ready-to-Eat Pepperoni Hot Pockets Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V011000·2021-01-15

    Ford Escape rear drive axle lubricant defect may cause loss of control

    Ford is recalling approximately 147 2020 Ford Escape vehicles and related models due to inadequate lubricant in the rear drive unit, which may cause the rear axle to seize and result in loss of vehicle control and crash risk.

    Product
    FORD — FORD, LINCOLN ESCAPE, CORSAIR, EDGE, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V013000·2021-01-15

    2021 KZRV Recreational Trailers Recalled for Improper Microwave Circuit Protection

    KZRV recalls 2021 Escape, Sonic, and Sportsmen Classic trailers with microwave circuits on improper 20-amp circuit breakers (should be 15-amp), creating fire risk. Owners should request free replacement from KZRV.

    Product
    KZRV — KZRV ESCAPE, SONIC, SPORTSMEN CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V010000·2021-01-14

    2019-2021 Honda Odyssey fuel tank assembly recall due to fire risk

    Braun Corporation is recalling certain 2018-2021 Honda Odyssey vehicles due to a fuel tank assembly defect that may cause fuel leaks, creating a potential fire risk. No injuries have been reported.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21719·2021-01-14

    Scalpa Numb Topical Anesthetic Cream Recalled for Child-Resistant Packaging Failure

    Scalpa Inc. is recalling Scalpa Numb Maximum Strength Topical Anesthetic Cream because the packaging does not meet child-resistant requirements, posing a poisoning risk to young children.

    Product
    Scalpa Numb Maximum Strength Topical Anesthetic Cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V009000·2021-01-14

    2021 Heartland Mallard recreational trailers recalled for suspension defect

    Heartland is recalling certain 2021 Mallard M180BH recreational trailers with incorrect axle, rims, and tires that can cause overloading and increase crash risk. Free replacement parts are available.

    Product
    HEARTLAND — HEARTLAND MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0203-2021·2021-01-13

    SCA Pharmaceuticals Recalls Neostigmine Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 390 syringes of neostigmine methylsulfate due to a lack of assurance of sterility and potential defective caps.

    Product
    neostigmine methylsulfate 5 mg/5 mL, (1mg/ml), Rx Only, 5 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004075009
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0212-2021·2021-01-13

    SCA Pharmaceuticals Recalls Succinylcholine Chloride Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 5,067 syringes of Succinylcholine Chloride 100 mg/5mL due to a lack of assurance of sterility and potential defective caps.

    Product
    SUCcinylcholine Chloride 100 mg/5mL, Rx Only, 5 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., WIndsor, CT, 06095, barcode 70004090809
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0204-2021·2021-01-13

    SCA Pharmaceuticals Recalls Phenylephrine Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 23,029 syringes of Phenylephrine HCl due to a lack of assurance of sterility and potential defective caps.

    Product
    PHENYLephrine HCl 1000 mcg/10 mL in 0.9% Sodium Chloride, (100 mcg/mL) Rx Only, 10 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004081012
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0197-2021·2021-01-13

    SCA Pharmaceuticals Recalls Ketamine Injection Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 11,075 syringes of Ketamine 100 mg/10mL injection due to a lack of assurance of sterility and potential defective syringe caps.

    Product
    Ketamine 100 mg/10mL in 0.9% Sodium Chloride Injection (10 mg/mL), CII, Rx Only, 10 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004043012
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0186-2021·2021-01-13

    SCA Pharmaceuticals Recalls Atropine Sulfate Injection Due to Sterility Concerns

    SCA Pharmaceuticals is recalling Atropine Sulfate Injection syringes due to a lack of assurance of sterility and potential defective caps.

    Product
    Atropine Sulfate Injection, 0.8 mg/2 mL (0.4 mg/mL), 2 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004004006
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0785-2021·2021-01-13

    Accuray Recalls TomoTherapy Systems Due to Potential Radiation Dose Rotation Error

    Accuray is recalling eight TomoTherapy Treatment Delivery Systems because an MLC tickle error may cause the delivered radiation dose to rotate from the planned dose.

    Product
    TomoTherapy Treatment Delivery System with iDMS - Product Usage: used as an integrated system for the planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0194-2021·2021-01-13

    SCA Pharmaceuticals Recalls Glycopyrrolate Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 1,614 syringes of Glycopyrrolate 1 mg/5mL due to a lack of assurance of sterility and potential defective caps.

    Product
    Glycopyrrolate 1 mg/5mL (0.2mg/mL), 5 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004063809
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0199-2021·2021-01-13

    SCA Pharmaceuticals Recalls Lidocaine HCl Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling Lidocaine HCl 1% syringes due to a lack of assurance of sterility and potential defective caps.

    Product
    Lidocaine HCl 1% 10 mL (10mg/ml), Rx Only, 1 mL Single Dose Syringe, SCA Pharma, Inc., 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004072012
    Category
    Drug
    Distribution
    Distributed nationwide