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.
Reported Jun 17, 2026
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co. LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2bones USA, LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INSPIREMD Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Atlan A350. Model Number: 8211500. anesthesia workstation
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hometown Food Company
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kico Knee Innovation Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculus Technologies
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported Jun 10, 2026
STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straus Family Creamery
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 10, 2026
1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Coffee Connexion Co., Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 27, 2026
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported May 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ghirardelli Chocolate Company
9 more products in this recall
FDA (openFDA food enforcement)
Reported May 27, 2026
Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Llorens Pharmaceuticals International Division, Inc.
FDA (openFDA food enforcement)
Reported May 27, 2026
Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (85G) bottle. UPC 8 50008-53861 2. Made by Pork King Good,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pork King Good, LLC
FDA (openFDA food enforcement)
Reported May 27, 2026
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tangent Endoscopy, LLC
FDA (openFDA device enforcement)
Reported May 20, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dexcom, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 20, 2026
Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Arizona recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.