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 Sep 10, 2025
Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Lemon Meringue Pie, 8" round. Net Wt. 27 OZ; Refrigerate after opening Item Code 31811; UPC: 8 85523 31811 1;Jessie's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jessie Lord Bakery, LLC
FDA (openFDA food enforcement)
Reported Sep 10, 2025
Medshape Universal Joints, REF: DNE-9000-UJ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medshape, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Salad Kit labeled as follows: Taylor FARMS Honey Balsamic SALAD KIT, NET WT. 8.3 OZ (235g), INGREDIENTS: HONEY BALSAMIC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms Retail, Inc.
FDA (openFDA food enforcement)
Reported Sep 3, 2025
Akreos, SKU: AO60P0300. Akreos intraocular lenses
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2025
Spectrum IQ Infusion Pump, Product Code 3570009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2025
BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Sep 3, 2025
Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2025
BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2025
STA Satellite. Product Code: All references. All software versions. The STA Satellite is a fully automated benchtop…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2025
IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Sep 3, 2025
ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS BOWED CANAL FILLING STEMS. Canal filling stem implants.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Onkos Surgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2025
Orascoptic Superior Visualization Custom loupes with Dragonfly frames
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orascoptic Surgical Acuity
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2025
Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The J.M. Smucker Company
FDA (openFDA food enforcement)
Reported Sep 3, 2025
Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.THOR Photomedicine Ltd.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2025
Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Aug 27, 2025
Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Khee Trading, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 27, 2025
Pentax Medical Video Processor; Model Number: EPK-i8020c;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Aug 20, 2025
a.) Actylis brand Lithium Orotate 4% packaged in HDPE Liner in a 25kg carton b.) Actylis brand Lithium Orotate 9%…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aceto US, L.L.C
FDA (openFDA food enforcement)
Reported Aug 20, 2025
FG60005 Blueberry Basil Lemonade
Moderate riskThis product could cause temporary or reversible health problems — stop using it.And Go Concepts dba Salad and Go
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 20, 2025
Duloxetine Delayed-Release Capsules, USP, 60 mg, 1,000 Capsules per bottle, Rx Only, Manufactured by: Towa…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breckenridge Pharmaceutical, Inc.
FDA (openFDA drug enforcement)
Reported Aug 20, 2025
Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefree Surgical Specialties
3 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.