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.
4,045 stored notices name Arizona, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,853 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Nov 13, 2013
Jim Dandy¿ Iron Fortified Quick Grits, 1lb paper box, Labeled in part "INGREDIENTS: IRON, WHITE CORN GRITS, NIACIN,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J M Smucker Co.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2013
Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the abdominal muscles.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pinook-Usa
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Angel Food Cake; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Safeway Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2013
GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 5, LEFT, QTY: (1), REF 71420168. Product Usage: orthopaedic
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre; 15248C-22/25 The Regional Anesthesia family of products is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Dekompressor Percutaneous Discectomy Probe. The Dekompressor is a single use disposable discectomy probe that passes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 13, 2013
VIT-RA-TOX Whole Beet Plant Juice, dietary supplement, dry, 400 mg tablet, packaged in 150 tablets glass, amber…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitalab Co. Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2013
P.F. Chang's Home Menu, Pork & Leek Dumplings, frozen, packaged in 12.5 oz bags. UPC: 0 36200 21215 8
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2013
Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2013
PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare It
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
HemoCue¿ Urine Albumin Microcuvettes, 25 Microcuvettes HemoCue AB Angelholm, Sweden The quantitative, rapid,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HemoCue AB
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012 Manufactured for: MAQUET Cardiopulmonary AG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Nov 6, 2013
PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower G.I. Endoscopes are provided with Air/Water…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pentax Medical Company
FDA (openFDA device enforcement)
Reported Oct 30, 2013
BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube, part # 245122, packaged in 100 ct cartons and labeled in part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Oct 30, 2013
Fruit Rush Black Cherry Artificially Flavored Fruit Drink, One Gallon, Plant 06-704
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dean Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 30, 2013
NatureMost LABORATORIES NATURAL WHEY POWER W / YERBA MATE VANILLA / ALMOND Dietary Supplement NET WEIGHT 3 LBS.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.NatureMost
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 30, 2013
Acuson SC2000 volume imaging ultrasound systems at software version 3.0. Mfg name: Siemens Medical Solutions USA, Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Disinfection
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft Delivery System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Harvest Technologies Corporation
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology and Brilliance CT 16 (Air) Brilliance CT Big Bore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R) Reagent Cartridge Lot 11349BB The Urinary /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Talenti German Chocolate Cake Gelato, One Pint (473 mL), Crafted By: Talenti, Marietta, GA 30062.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Talenti Gelato
FDA (openFDA food enforcement)
Reported Oct 9, 2013
Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of interventional and/or diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Arizona recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.