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.
4,035 stored notices name Arizona, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Apr 1, 2026
SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 "…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Siluetaya, LLC
FDA (openFDA food enforcement)
Reported Apr 1, 2026
Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT NET WT 16OZ UPC 0 70852 54400 7 & 32OZ UPC 0 70852 54200 3 DISTRIBUTED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Saputo Cheese USA, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 25, 2026
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Winder Laboratories, LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2026
DxC 700 AU, REF: B86444, B86446
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Life Sciences
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Palmetto Gourmet Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 18, 2026
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Mar 18, 2026
C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tipp Distributors, Inc. dba Novamex
FDA (openFDA food enforcement)
Reported Mar 11, 2026
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascutek, Ltd.
FDA (openFDA device enforcement)
Reported Mar 4, 2026
PIE Trolley System Model: 2005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edermy LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2026
MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MRIMed Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2026
Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Prime Food Processing LLC.
FDA (openFDA food enforcement)
Reported Mar 4, 2026
Campy CVA Medium 100/PK, R01272
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel, Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health, Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
FDA (openFDA food enforcement)
Reported Feb 25, 2026
MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2026
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
1 more product in this recall
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.