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 48,122 notices were distributed nationwide, so they reach Arizona too — those are in the archive.

Medical devices

Reported Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2019

Kroger Wild Caught Sockeye Salmon Boneless, Frozen, Raw, Skin-on, not ready to eat (NRTE), individually vacuum packed…

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

Cold Locker Processing LLC

FDA (openFDA food enforcement)

Food

Reported Nov 13, 2019

Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose…

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

Helena Laboratories, Corp.

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2019

Cranberry Chicken Salad, Tuscan Sun brand, is a ready to eat sandwich. Net wt. 9.3 oz (263g). UPC 0 43701 01414 3.…

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

Jumbo Foods, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is an integrated delivery…

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

Western / Scott Fetzer Company

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

C3 Wave App, v. 2.0.5

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…

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

OrthoPediatrics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…

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

Pajunk GmbH

FDA (openFDA device enforcement)

Meat & poultry

Reported Nov 6, 2019

Simmons Prepared Foods, Inc. Retira Productos De Aves Debido A Una Posible Contaminación Con Materia Extraña

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

Simmons Prepared Foods, Inc.

USDA FSIS

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

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

Candela Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole Packaged Foods, LLC Westlake Village, CA 91361…

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

Dole Packaged Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

The ICS CHARTR EP 200

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Irrisept Wound Debridement and Cleansing System. 12 units per case.

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

IrriMAX Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 OEM Customer Software: Sentosa SQ Suite Software…

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

Life Technologies Holdings Pte Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029;…

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

Roland Foods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…

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

Smiths Medical ASD Inc.

1 more product in this recall

FDA (openFDA device enforcement)

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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.