State

Arizona product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19976–20000 of 81753

SevereFDA (Devices)·Z-0076-2023·2022-10-26
Medical gas filter recalled due to splitting and detachment risk
TELEFLEX LLC is recalling Iso-Gard Filter S medical gas filters due to incidents of device splitting or detaching during use. The affected filters may compromise patient safety.
Product
Iso-Gard Filter S with Expandi-Flex/Elbow: a) REF 19012, OUS only, b) REF 19012T with Tethered Cap, OUS only; Microbial medical gas filter, single-use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0077-2023·2022-10-26
Teleflex Catheter Mount and Filter May Split or Detach During Use
Catheter mounts with filters (REF 191667-000100) used to connect endotracheal tubes or masks to breathing circuits may split or detach during patient use. Teleflex is recalling affected units distributed nationwide.
Product
Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection (Endotracheal tube and mask)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0072-2023·2022-10-26
Iso-Gard Filter S Recalled for Device Splitting or Detachment During Use
Teleflex is recalling Iso-Gard Filter S microbial filters (60,500 units) due to incidents of device splitting or detaching during use. The filters protect patients and equipment from bacterial and viral contamination in breathing systems.
Product
Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral filters for use in breathing system for the protection of patient and equipment.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0073-2023·2022-10-26
Iso-Gard Filter S Medical Gas Filter Recall Due to Splitting or Detachment
TELEFLEX LLC is recalling Iso-Gard Filter S microbial medical gas filters due to incidents where the device may split or detach during use. The FDA classified this as a Class I recall.
Product
Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medical gas filter, single-use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0094-2023·2022-10-26
N Antiserum to Human IgG Fails High-Dose Hook Effect Performance Standards
Siemens N Antiserum to Human IgG reagent batches are not meeting performance standards for high-dose immunoassay testing. The issue affects 10,201 packs distributed nationwide and may result in inaccurate diagnostic test results.
Product
N Antiserum to Human IgG, 5mL Variant for BN II System and BN ProSpec System- IVD Siemens Material Number (SMN): 10446299
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0106-2023·2022-10-26
Chest Tube Insertion Tray Recalled Due to Over-Sterilization of Suture Component
Medline recalls CENTURION SnagFree Chest Tube insertion trays because a silk suture component was sterilized twice instead of once, potentially compromising its integrity. The affected lot contains 18 kits distributed in California and Texas.
Product
CENTURION SnagFree Chest Tube insertion Tray, Reorder CHT545
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0116-2023·2022-10-26
Abbott MitraClip and TriClip Clip Delivery Systems: Locking Malfunction Risk
Abbott is recalling MitraClip and TriClip Clip Delivery Systems due to clip locking malfunctions. Failed procedures may result in mitral regurgitation recurrence, device embolization, or tissue injury.
Product
Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR, MitraClip NTR Clip Delivery System CE/CDS0602-NTR, MitraClip XTR Clip Delivery System CE/CDS0602-XTR, MitraClip G4 Clip Delivery System NT CE/CDS0702-NT, MitraClip G4 Clip Delivery System NTW CE/CDS0702-NTW…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0115-2023·2022-10-26
MitraClip Clip Delivery System Recalled for Locking Malfunctions
Abbott Vascular is recalling MitraClip Clip Delivery System devices due to observed increases in clip locking malfunctions that can lead to recurrence of mitral regurgitation, device embolization, or tissue injury.
Product
Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT, MitraClip G4 Clip Delivery System NTW US/CDS0701-NTW, MitraClip G4 Clip Delivery System XT US/CDS0701-XT, MitraClip G4 Clip Delivery System XTW…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0099-2023·2022-10-26
Surgical Implant Kit Recall: Incorrect Drill Guide Included
Synthes surgical implant kits are being recalled because they contain an incorrect size drill guide that cannot properly prepare the bone for the implant, creating a risk of bone damage during surgery.
Product
SPEED 15X12X12mm Continuous Compression Implant, Product No. SE-1512
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0063-2023·2022-10-26
Lyons Ready Care Thickened Orange Juice recalled for spoilage
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Juice 46 fl oz cartons due to indication of product spoilage. Specific lot numbers distributed nationwide are affected.
Product
Lyons Ready Care Thickened Orange Juice packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Food)·F-0054-2023·2022-10-26
Lyons Ready Care Thickened Apple Honey Nectar Recalled Due to Spoilage
Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Honey Nectar due to indications of product spoilage. The nationwide recall affects 645 cases with specific lot numbers and best-by dates in March 2023.
Product
Lyons Ready Care Thickened Apple Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Devices)·Z-0100-2023·2022-10-26
Synthes SPEED implant recall: drill guide size mismatch in surgical kit
Synthes is recalling SPEED 9X10X10mm surgical implant kits nationwide due to an incorrect-size drill guide that will not properly prepare bone for the implant, creating potential for bone damage.
Product
SPEED 9X10X10mm Continuous Compression Implant, Product No. SE-0910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0112-2023·2022-10-26
Medicina Reusable Oral Syringe Recalled for Unapproved Plunger Material
Medicina Uk Ltd is recalling Medicina Reusable Oral syringes because the plunger was manufactured with polyethylene instead of the required polypropylene material. The 11,100 affected syringes do not meet raw material specifications.
Product
Medicina Reusable Oral syringe 1ml Code: OTH01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0113-2023·2022-10-26
Reusable Oral Syringe Recalled for Unapproved Plunger Material
Medicina UK Ltd is recalling Reusable Oral Syringes because plungers were manufactured from unapproved polyethylene instead of the specified polypropylene material.
Product
Medicina Reusable Oral syringe 5ml Code: OTH05
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0068-2023·2022-10-26
Tastykake Glazed Caramel Apple Pie Recalled for Undeclared Soy
Flowers Foods is recalling Tastykake Glazed Caramel Apple Pie because some packages contain undeclared soy lecithin, a major food allergen. Consumers with soy allergies should not consume this product.
Product
TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 08618 6 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-0102-2023·2022-10-26
ARROW Midline Catheter Kit Mislabeled with Wrong Device Type
ARROW INTERNATIONAL Inc. is recalling an ARROW Pressure Injectable Arrowgard Blue Advance Midline Catheter Kit due to mislabeling. The package labels incorrectly specify a double-lumen 5.5 French catheter, but the kit contains a single-lumen 4.5 French catheter.
Product
ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF ASK-41552-JHVA1. For peripheral access to the venous system for intravenous therapy, blood sampling, infusion, and pressure injection of contrast media.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0060-2023·2022-10-26
Lyons Magnus Thickened Cranberry Cocktail Nectar Recalled for Product Spoilage
Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Nectar due to indication of product spoilage. Approximately 2094 cases were distributed nationwide.
Product
Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighFDA (Devices)·Z-0092-2023·2022-10-26
IV extension set recall for potential joint failure and leakage risk
B. Braun is recalling CARESITE SMALLBORE EXT SET T-PORT 5 IN. devices due to potential bonded joint failure that could cause leakage or detachment during use. The malfunction may result in delayed therapy, bloodstream infection risk, and exposure to hazardous medications.
Product
CARESITE SMALLBORE EXT SET T-PORT 5 IN., Product Code 470114, 100 units per carton. The A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0043-2023·2022-10-26
Market Pantry White Fudge Animal Cookies Recalled for Metal Contamination
Market Pantry White Fudge Animal Cookies sold at Target may contain metal fragments. D. F. Stauffer Biscuit Co is recalling 883 cases distributed nationwide.
Product
White frosted animal cookies with multi-colored non-pareils in a 44oz plastic jug labeled "Market Pantry White Fudge Animal Cookies"
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0048-2023·2022-10-26
Seeking Health Optimal Multivitamin Chewable Supplement Recalled for Excess Copper
Seeking Health LLC is recalling Optimal Multivitamin Chewable Dietary Supplement tablets because lab testing found higher copper levels than stated on the label.
Product
Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 810007520902. Product labels read in part: Adults and children age 4 and over; Chew 2 tablets daily.…
Category
Consumer Product
Distribution
51 states
HighFDA (Food)·F-0061-2023·2022-10-26
Imperial Thickened Cranberry Cocktail Honey Recalled for Product Spoilage
Lyons Magnus is recalling Imperial Thickened Cranberry Cocktail Honey due to indication of product spoilage. Consumers who have purchased affected cases should stop using the product.
Product
Imperial Thickened Cranberry Cocktail Honey packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
Category
Food
Distribution
48 states
HighNHTSA·22V804000·2022-10-26
Rearview camera display malfunction in 2022 Lamborghini Urus vehicles
The infotainment system in certain 2022 Lamborghini Urus vehicles may become damaged, causing the rearview camera display to become inoperative. This reduces rear visibility and increases the risk of a crash.
Product
LAMBORGHINI — LAMBORGHINI URUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0066-2023·2022-10-26
Mrs. Freshley's Cherry Fruit Pie recalled for undeclared soy lecithin
Flowers Foods is recalling Mrs. Freshley's Cherry Fruit Pie due to undeclared soy lecithin. Soy is a major allergen; consumers with soy allergies should not consume the product.
Product
Mrs. Freshley's Cherry Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 0081 0 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084
Category
Food
Distribution
50 states
HighFDA (Food)·F-0046-2023·2022-10-26
Nick's Krispi Nougat Protein Bar Recalled for Undeclared Hazelnut
Nick's Krispi Nougat Protein Bar is being recalled because the product contains hazelnuts that are not declared on the label. This poses a risk to consumers with tree nut allergies.
Product
Nick's Krispi Nougat Protein Bar, 1.76 oz., in foil wrapper in 12 pack boxes. UPC: 00850009682345 Product of North Macedonia Distributed by LUB Foods USA, Inc. El Segundo, CA 90245
Category
Food
Distribution
12 states
HighNHTSA·22V806000·2022-10-26
Multiple 2021-2022 Audi models recalled for rearview camera failure
Volkswagen Group of America is recalling certain 2021-2022 Audi vehicles. The infotainment system may fail to display the rearview camera, reducing rear visibility and increasing crash risk.
Product
AUDI — AUDI A3, Q8, Q3, Q7
Category
Vehicle
Distribution
Distributed nationwide