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.

23151–23175 of 81775

HighFDA (Food)·F-0893-2022·2022-03-23
Basil Pesto Bowtie Pasta Salad Kits Recalled for Hard Plastic Contamination
Fresh Creative Foods is recalling Basil Pesto Bowtie Pasta Salad Kits because hard clear plastic pieces were found in the product during manufacturing. The plastic originated from ice purchased from the manufacturer's supplier.
Product
Fresh Creative Foods; BASIL PESTO BOWTIE PASTA SALAD DIRECT KIT 2/5.15625 LB UPC: 10013454380922; Item # 404736 Perishable/ Keep Refrigerated Kit components: 2/3 lb. bags of Bowtie Pasta, 2/24 oz. bags of Sweet Basil Dressing, 2/8 oz. bags of diced sundried tomato, 2/2.5 bags…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0791-2022·2022-03-23
Lumbar Puncture Tray Pediatric Recalled Due to Manometer Failure
Bard Peripheral Vascular Inc is recalling pediatric lumbar puncture trays due to manometer leaking and mating failures that could prevent proper pressure measurement during procedures.
Product
LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0868-2022·2022-03-23
Rosarita Organic Refried Beans recalled for small rocks contamination
ConAgra Foods is recalling Rosarita Organic Refried Beans due to possible contamination with small rocks. The recall affects approximately 169,680 cases distributed across seven states.
Product
Rosarita Organic Refried Beans Multipack carton containing 8 - 16oz cans
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-0781-2022·2022-03-23
Boston Scientific RX Cholangiogram Kit Recall Due to Sterile Barrier Breach
Boston Scientific is recalling RX Cholangiogram Kits because the sterile barrier has been breached, compromising the sterility of the devices. The affected kits were distributed worldwide.
Product
RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280 M00575320 M00575360 M00575380 M00575400 M00575440 M00575480
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0766-2022·2022-03-23
Boston Scientific recalls 68 medical devices with sterility breach
Boston Scientific is recalling 68 JAGTOME REVOLUTION RX medical devices due to sterile barrier breach. The devices were distributed worldwide including throughout the US.
Product
JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2022·2022-03-23
HYDRATOME RX surgical device recalled due to sterile barrier breach
Boston Scientific recalls 251 HYDRATOME RX 44-30MM/450CM units worldwide due to sterile barrier breach that compromises device sterility.
Product
HYDRATOME RX 44-30MM/450CM Material Number: M00583070
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0790-2022·2022-03-23
FDA Recalls Safe-T PLUS Pediatric Lumbar Puncture Tray Due to Manometer Failure
Bard Peripheral Vascular Inc is recalling 20,400 Safe-T PLUS pediatric lumbar puncture trays due to manometer leaking and mating failures. The devices were distributed nationwide and internationally to healthcare facilities.
Product
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2022·2022-03-23
Medical Device Recall: Boston Scientific JAGTOME RX Sterile Barrier Breach
Boston Scientific is recalling 98 units of the JAGTOME RX 39-30-260-025 medical device due to compromised sterile barrier that affects device sterility. Units were distributed worldwide.
Product
JAGTOME RX 39-30-260-025 Material Number: M00573100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2022·2022-03-23
Boston Scientific JAGTOME RX Recalled for Sterile Barrier Breach
Boston Scientific is recalling 96 units of JAGTOME RX medical devices due to a sterile barrier breach that compromises device sterility. Patients should contact their physician if they received this device.
Product
JAGTOME RX 49-30-260-035 Material Number: M00573020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0891-2022·2022-03-23
Broccoli Cheddar Pasta Salad Recalled Due to Hard Plastic Contamination
Walmart's Freshness Guaranteed Broccoli Cheddar Pasta Salad is recalled due to hard plastic pieces found during manufacturing. The contamination came from ice purchased from a supplier and affects products with use-by dates of March 14–22, 2022.
Product
Freshness Guaranteed BROCCOLI CHEDDAR PASTA SALAD WM 6/14 OZ (397 g) UPC: 0 78742 37256 3 Distributed by Walmart Inc., Bentonville, AR 72716
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0776-2022·2022-03-23
Medical Device Sterile Barrier Breach: JAGTOME RX Recall
Boston Scientific is recalling JAGTOME RX medical devices because the sterile barrier may be compromised, which could allow contamination. The recall affects 163 units distributed worldwide.
Product
JAGTOME RX 44-30-450-035 Material Number: M00573070
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0788-2022·2022-03-23
LYFO Disk Quality Control Product Recalled for Organism Mislabeling
Microbiologics Inc recalls LYFO Disk lot 983-40-3 because it is labeled as Candida tropicalis but actually contains Yersinia enterocolitica. The mislabeling may cause laboratory quality control failures and delayed test results.
Product
LYFO Disk
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0805-2022·2022-03-23
Calcium Alginate Wound Dressings Recalled for Incorrect Instructions
CellEra LLC is recalling Vitale Silver calcium alginate dressings nationwide because packages contain incorrect Instructions for Use with language not approved by the FDA. The firm is providing replacement packages with corrected instructions.
Product
20548 Vitale Silver calcium Alginate Dressings 4x8, 5/box
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0784-2022·2022-03-23
Mycoplasma genitalium Control Panel Distributed Without Proper Release Testing
Microbiologics Inc is recalling Mycoplasma genitalium Control Panel units that did not undergo proper release testing before distribution. Affected lots were distributed across the U.S. and internationally.
Product
Mycoplasma genitalium Control Panel (Inactivated Pellet)
Category
Medical Device
Distribution
18 states
ModerateFDA (Drugs)·D-0653-2022·2022-03-23
hydrALAZINE HCl Tablets 10 mg Recalled for Failed Impurity Specifications
The Harvard Drug Group is recalling hydrALAZINE HCl Tablets, USP, 10 mg due to failed impurity and degradation specifications detected during routine stability testing. The recall affects 5,953 cartons distributed nationwide.
Product
hydrALAZINE HCl Tablets, USP, 10 mg, 100 Tablets per carton (10x10 blister packs), Rx only, Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152 USA. NDC # 0904-6440-61
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0802-2022·2022-03-23
Calcium Alginate Wound Dressings Recalled for Incorrect Instructions
CellEra LLC is recalling Vitale Silver calcium alginate wound dressings nationwide due to incorrect instructions for use containing language beyond FDA-cleared content.
Product
20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0804-2022·2022-03-23
Calcium alginate wound dressings recalled for incorrect instruction labeling
CellEra LLC is recalling Vitale Silver calcium alginate dressings because the included Instructions for Use contain language exceeding FDA clearance. The firm is replacing affected units with correct instructions.
Product
20545 Vitale Silver calcium Alginate Dressings 4x5, 10/box
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0801-2022·2022-03-23
Medical dressing recall issued due to incorrect instructions for use
CellEra LLC recalls Vitale Silver calcium Alginate Dressing Ropes due to incorrect Instructions for Use in product packaging. The manufacturer is replacing affected units with corrected instructions.
Product
20500 Vitale Silver calcium Alginate Dressing Ropes, 5/box
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0803-2022·2022-03-23
Medical device wound dressing recall for incorrect instructions
CellEra LLC is recalling Vitale Silver calcium Alginate Dressings because product packages contain incorrect Instructions for Use with language beyond FDA 510(k) clearance scope. The firm is replacing affected units with correct instructions.
Product
20544 Vitale Silver calcium Alginate Dressings 4x4, 10/box
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V172000·2022-03-22
Marion Body Works Recalls 2018 International SR525 Emergency Vehicle
Marion Body Works is recalling one 2018 International SR525 emergency vehicle because the engine may overcome the parking brake, increasing crash risk.
Product
MARION BODY WORKS — MARION BODY WORKS INTERNATIONAL SR525
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V173000·2022-03-22
Hi-Tech E.V.S. Recalls Spartan Emergency Vehicles for Display Defect
Hi-Tech E.V.S. is recalling 2020 Spartan MetroStar and 2021 Spartan Gladiator emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.
Product
HI-TECH E.V.S. — HI-TECH E.V.S. SPARTAN METROSTAR, SPARTAN GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E024000·2022-03-22
LeMans Recalls Replacement Motorcycle Rear Wheels Due to Spoke Breakage Risk
LeMans is recalling specific replacement laced motorcycle rear wheels because incorrect welding may cause spokes to break, increasing the risk of a crash.
Product
WHEELS:SPOKES recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V170000·2022-03-21
2022 Heartland Travel Trailers Recalled for Electrical Fire Risk
Heartland is recalling certain 2022 Trail Runner, Prowler, and Lithium travel trailers with defective power inlet bolts that may loosen, creating an electrical fire hazard. Dealers will inspect and replace the inlet free of charge.
Product
HEARTLAND — HEARTLAND PROWLER, LITHIUM, TRAIL RUNNER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E023000·2022-03-19
ZH Brothers Recalls Epicord 50-amp Shore Power Inlets Due to Fire Risk
ZH Brothers is recalling Epicord 50-amp Shore Power Inlets because loose wiring connections may cause electrical arcs or shorts, increasing the risk of fire.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V168000·2022-03-18
Mercedes-Benz Recalls Vehicles for Software Configuration Errors
Mercedes-Benz is recalling specific 2007-2014 models because incorrect software updates may cause loss of drive power or control functions, increasing crash risk.
Product
MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ SLK350, E350, G550, SLK280
Category
Vehicle
Distribution
Distributed nationwide