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.
4,036 stored notices name Arizona, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Jan 22, 2025
DELI FRESH VEGETABLE TRAY MED, 4 lb., packaged in a plastic container with a plastic lid, UPC 11110-99274
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 15, 2025
Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aerin Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
EnVisio Patient Pad Transition Cushion, Model/Catalog Number: ENVISIO-SYS Product Description: The EnVisio Patient Pad…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elucent Medical Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nipro Renal Soultions USA, Corporation
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2025
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Unitek Corporation
FDA (openFDA device enforcement)
Reported Jan 8, 2025
AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2025
whole fresh American cucumbers packaged in bulk cardboard containers labeled with the "Pamela" brand, a generic white…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baloian Farms
FDA (openFDA food enforcement)
Reported Jan 8, 2025
Product is a whole, fresh cucumber with no individual packaging, labeling, PLU, or other identifying information.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Delta Fresh LLC.
FDA (openFDA food enforcement)
Reported Jan 8, 2025
--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grimmway Enterprises, Inc. dba Grimmway Farms
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 8, 2025
Beef & Lamb Gyro Sandwich Express Meal Kit. Net wt. 31.8oz. UPC 0 13454 38313 1. Each kit contains 6 Pitas, Gyro Meat,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 8, 2025
Sprout Gyro Family Kit, net wt. 1.750 lb (794 g), food, perishable, plastic tray, 28oz, U UPC 20594800000.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sprouts Farmers Market
FDA (openFDA food enforcement)
Reported Jan 1, 2025
The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
FDA (openFDA device enforcement)
Reported Jan 1, 2025
20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2025
FACSLyric 2L4C Instrument US, Catalog Number 662875, UDI 00382906628756 BD FACSLyric" flow cytometer is intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Bio Sciences
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2025
BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Borsari Food Company Inc.
FDA (openFDA food enforcement)
Reported Jan 1, 2025
BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straight Smile, LLC
FDA (openFDA device enforcement)
Reported Jan 1, 2025
ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zoe US, Inc.
FDA (openFDA food enforcement)
Reported Dec 25, 2024
WHOLE FOODS MARKET, Organic Carrot Sticks, NET WT. 15 oz (425 g), PERISHABLE KEEP REFRIGERATED, Packed For: Whole Foods…
High riskUsing this product could cause serious injury, illness or death — stop using it now.F&S Fresh Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 25, 2024
OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Duravent Silicone Ventilation Tube. Model Number: 240075.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Dec 19, 2024
Nail Factory Recalls Ineligible Frozen Siluriformes Fish Products Imported From Vietnam
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nail Factory
USDA FSIS
Reported Dec 18, 2024
BD Pyxis MedStation ES, REF: 323
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
2 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.