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 Feb 20, 2013
Chenica Gunnell Rehab Series of Wheelchairs (GRSW); Mechanical Wheelchair, Sold as Rehab Tough and Tilt (TNT), Rehab…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chenica Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2013
GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The T-piece Resuscitation System [ventilator, emergency…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2013
The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or endoscopic visualization for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lumenis Limited
FDA (openFDA device enforcement)
Reported Feb 20, 2013
Stringless Sugar Snap Peas, Sunny Shores' Mann's. Net Wt 8 oz (227 g); Perishable, Preservative Free, keep…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mann Packing Co. Inc.
FDA (openFDA food enforcement)
Reported Feb 20, 2013
Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Feb 20, 2013
Pamela's Baking and Pancake Mix; Gluten Free, Wheat Free 24 oz package. UPC 93709-30010 Pamela's Products, Ukiah, CA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pamela's Products, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2013
St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St Jude Medical Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diagnostic Hybrids Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Medacta Quadra Trial Broach size 0 part # 01.10.10.045, for use with the Medacta Total Hip Prosthesis System. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage: Universal Fluoroscopic Applications
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2013
BacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No EX500, EX600, and EX700. Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Esteem Programmer Model 6001, US and ISA, Model 3001 Dell E54XX, part of the Esteem Totally Implantable Hearing System.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Envoy Medical Corporation
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated for bipolar coagulation and mechanical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Extremity Medical, IO FiX System Accessory. Catalog Number 101-00010. This screw measuring device is an accessory to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Feb 6, 2013
Betty Croker, Super Moist Cake Mix, Golden Vanilla, NET WT 15.25 oz (432 g), UPC 0 16000 40993 4, Dist by General Mills…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Feb 6, 2013
Island Delights Coconut Haystack Candy Maple Natural Flavor Coconut Haystacks, NET WEIGHT 2 OZ, 4 oz and 8 oz clear…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Island Delights, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 6, 2013
Spice Cake Mix , 25 lb. and 50 lb. kraft bags, labelled a) CMC Quality and Value, Spice Cake Mix, 46702-00985, NET Wt.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jiffy Food Service, LLC
FDA (openFDA food enforcement)
Reported Jan 30, 2013
Becton, Dickinson and Company, BBL Crystal Enteric/Nonfermenter ID Kit, Catalog # 24500, cartons of 20 kits, In-vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2013
DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Code: 1867-15-870 Spinal Implant Component.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2013
Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***BLACK BEAR***of the BLACK FOREST*** Naturally…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Marine Harvest USA, LLC
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 30, 2013
Roche COBAS INTEGRA 400 and 400 plus Analyzer, an in vitro diagnostic analyzer.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 23, 2013
Cold-smoked salmon in vacuum plastic bags that are partially clear and partially colored black, white, gold and pink.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ocean Beauty Seafoods, LLC
1 more product in this recall
FDA (openFDA food 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.