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.

Food

Reported Jul 23, 2025

Red cabbage, shredded packed in polybag and cardboard case. 14 lbs per case.

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

And Go Concepts dba Salad and Go

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2025

Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 10MM, VE Model/Catalog…

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

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2025

SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2025

i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.

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

Intersurgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2025

Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier I Model/Catalog…

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

Ortho-Clinical Diagnostics, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2025

Chocolate Crunch Cake Bar (85000), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master…

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

Rich Ice Cream Co.

9 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 23, 2025

Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik…

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

World Market Management Services, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog…

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

Alcon Research LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software…

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

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2025

TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Stratasys Ltd.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 16, 2025

Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases

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

Weaver Nut Company, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 9, 2025

--- Shell Eggs; Brown; Various sizes - medium, large, and jumbo; Various pack sizes - 5, 12, 18, and Loose ---- Clover…

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

August Egg Company

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2025

REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only, IVD. Used in flow cytometry for fluorescence…

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

Becton, Dickinson and Company, BD Bio Sciences

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF:…

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

C.R. Bard Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No.…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

Brand Name: Valeda Light Delivery System Product Name: Light Based Device for Dry Age Related Macular Degeneration…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Lumithera Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2025

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…

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

Peak Cocktails

FDA (openFDA food enforcement)

Medical devices

Reported Jul 2, 2025

REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY

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

Becton Dickinson Infusion Therapy Systems, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Spectral CT. Computed tomography X-ray system.

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 25, 2025

Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…

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 Jun 25, 2025

Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in…

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

Preat Corp.

FDA (openFDA device enforcement)

Food

Reported Jun 25, 2025

Topo Chico MINERAL WATER CARBONATED 16.9 FL OZ (500mL) Bottle UPC 0 21136 18061 9, Case UPC 0 21136 18062 6 MADE IN…

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

The Coca-Cola Company

FDA (openFDA food enforcement)

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Other states

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.