All recall categories

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.

Medical devices

Reported Oct 13, 2021

Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ZOLL Circulation, Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Molecular, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 6, 2021

Dairy Free Co. Dollup Lama Sour & Creamy Cashew Topping 4oz, 6 containers per case

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Central Kitchen Food Hub

FDA (openFDA food enforcement)

Medical devices

Reported Oct 6, 2021

Corin TriFit TS, Size 8, Standard Tapered Stem, REF 694.0008, Sterile.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Corin Ltd.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

OctoStretch with Stretch Leveller - The combination of this products allows the user to easily adjust/control the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hill-Rom, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT PACK, REF C74339 Access SARS-CoV-2 IgG (1st…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

In2bones USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 29, 2021

Banquet Cut European Style Cold Smoked Salmon, Item Number 2-92845, brand Gerard and Dominique Seafoods, packaged in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seabear Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 22, 2021

Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring function

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arjohuntleigh Magog, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carefusion

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Food

Reported Sep 22, 2021

Vita Aid Keto-Elemental Nutrition (Chocolate), VA-958. The product is a powder, packaged in an aluminum bag , with a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Naturo Aid Pharmaceutical Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Sep 22, 2021

MIC+Methyl B12 injection Methionine Inositol Choline+Methylcobalamin 25 mg/50 mg/50 mg/1 mg/mL, 10 mL vial sterile, Rx…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Promise Pharmacy, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 15, 2021

Nihon Kohden NKV-550 Ventilator, REF: NKV-550-U, CE 0344, UDI: (01) 00843685100012 The Nihon Kohden NKV-550 Series…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nihon Kohden Orangemed, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 8, 2021

Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hostess Brands, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 8, 2021

Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 8, 2021

CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Versea Diagnostics LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 8, 2021

CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zeltiq Aesthetics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cardinal Health

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.