All recall categories

Recalls distributed in Arizona

These notices name Arizona in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

3,983 stored notices name Arizona, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Arizona too — those are in the archive.

Medical devices

Reported Mar 13, 2024

MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC* Gastric-Jejunal Feeding Tube Kit with ENFit Connector…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Avanos Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2024

MRI system: Vantage Orian, Vantage Fortian, Model: MRT-1550

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Canon Medical System, USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2024

BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower, REF: 352;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 13, 2024

Frios Gourmet Pops - Banana Pudding Popsicle 3oz frozen popsicle packaged individually in clear plastic sleeve. 48…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

FGP Manufacturing, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 13, 2024

BANH PIA Hopia Cake, Mung Bean - Durian, 16.8 oz (480g)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

LQNN Inc.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2024

The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Micro Therapeutics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 13, 2024

Taylor Farms Pacific Recalls Kroger Brand Ready-To-Eat Apple Walnut With Chicken Salad Bowl Products Due to Misbranding…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Taylor Farm - Pacific

USDA FSIS

Medical devices

Reported Mar 6, 2024

IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF SA Graft Bolt, 08.5 x…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alphatec Spine, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2024

Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medtronic Neurosurgery

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2024

MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mutti USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2024

NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

NxStage MDS Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2024

Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Parker Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2024

Marketside Southwest Chopped Kit 10.3 oz. UPC 681131305129

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Ready Pac Foods Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2024

Cotija cheese packaged in the following configurations: 1. Sargento Course Grated Cotija Cheese Pack Size 6/5 lb.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sargento Foods, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2024

ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

World Green Nutrition Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 28, 2024

Baxter Exactamix Pro 1200, REF EXM12DY

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Baxter Healthcare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 28, 2024

Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Procter & Gamble Company

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2024

Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2024

Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

U.S. Tov, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 14, 2024

Neurovascular embolization device. The Optima Coil System is a series specialized coils that are inserted into the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Balt USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

FilmArray Pneumonia Panel Plus (Pneumoplus), REF: RFIT-ASY-0143, CED 2797, IVD, Rx Only (30 test kit)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 14, 2024

Flow-i C20 Anesthesia System, model 6677200

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge USA Sales Inc.

4 more products in this recall

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.