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.
4,042 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Nov 17, 2021
NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Health Group Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 10, 2021
3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape, Catalog No. 2244, (3M ID (SKU): 70-2011-8506-6,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Nov 10, 2021
Cedar s Organic Mediterranean Hommus 10 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cedar's Mediterranean Foods, Inc.
FDA (openFDA food enforcement)
Reported Nov 10, 2021
Flexor Check-Flo Introducer, Introducer Set, RPN KCFW-6.0-35-45-RB, GPN G09908 The introducer sheath incorporates a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 10, 2021
ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 10, 2021
FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Nov 10, 2021
IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lumenis, Inc.
FDA (openFDA device enforcement)
Reported Nov 10, 2021
Whole raw RED onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ProSource Produce LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 3, 2021
Calcium Chloride, 100 mg/mL MDV INJ, Rx only, Red Mountain Compounding Rx
Moderate riskThis product could cause temporary or reversible health problems — stop using it.First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
39 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 3, 2021
Simply Nature Organic Poppy Seed Dressing
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schlotterbeck & Foss LLC
FDA (openFDA food enforcement)
Reported Nov 3, 2021
Almond Flour Crackers fine ground sea salt packaged in a white box with yellow graphics weighing 4.25 oz. Label reads…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simple Mills
FDA (openFDA food enforcement)
Reported Nov 3, 2021
REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 3, 2021
Concerto User Interface Software provided with the following systems: (1) Xstrahl 100 Electronic Brachytherapy - 100kV…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xstrahl Limited
FDA (openFDA device enforcement)
Reported Oct 27, 2021
SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Oct 27, 2021
SIGNA Premier nuclear magnetic resonance imaging system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 27, 2021
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls (IVD)- For use in monitoring the performance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho Clinical Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Oct 27, 2021
EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Oct 27, 2021
Atellica IM 1300 Analyzer, SMN 11066001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 27, 2021
Tenaculum, Plastic
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Medical, LLC dba Stradis Healthcare
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 20, 2021
Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best by dates of SEPT 03 24 and SEPT 06 24, due…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B&G Foods North America, Inc.
FDA (openFDA food enforcement)
Reported Oct 20, 2021
BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with ANA Screen Reagent Packs/ANA Kits, REF: 665-1150;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Oct 20, 2021
Elekta Medical Linear Accelerator (EMLA), configured as follows: a. Elekta Precise Digital Accelerator; b. Elekta…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Oct 20, 2021
FAIRLIFE MILK 8OZ / 6PK CHOCOLATE (multi-pack format of small single serve bottle); Date Code "MAY2722 FA"; Case UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairlife LLC
FDA (openFDA food enforcement)
Reported Oct 20, 2021
Flower Drill Bit Kit 2.0 mm - intended to be used with solid 2.0mm screws and can be used with any plate that has been…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flower Orthopedics Corporation
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.