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 Aug 1, 2012
BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bridgepoint Medical
FDA (openFDA device enforcement)
Reported Aug 1, 2012
The Handi-Fil Disposable Syringe Fill Tube is a sterile plastic tube, approximately 10 inches in length, with a "J"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mallinckrodt Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2012
Sonoran Rice, 14 lbs (224 oz). Chonita Foods 847 E. 18th St. Tucson, AZ 85719.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Namias dba Chonita Foods
FDA (openFDA food enforcement)
Reported Aug 1, 2012
Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or intermittent…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics, Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2012
4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 REF 04.019.038S Manufactured or Distributed by…
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 Aug 1, 2012
.***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2012
PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tripath Imaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
CareFusion EnVe Ventilator Designed for use on patients who require respiratory support or mechanical ventilation and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 203, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra Limited
FDA (openFDA device enforcement)
Reported Jul 25, 2012
Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2012
SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Standard Process, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 25, 2012
SunOpta, Canadian Harvest Oat Fiber, Oat Fiber 300-33, Manufactured by SunOpta Ingredients, Chelmsford, MA 01824
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SunOpta Ingredients Group (Corporate HQ)
FDA (openFDA food enforcement)
Reported Jul 25, 2012
Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 is indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2012
Jimmy Peppers Hot Cherry Sliced Peppers, 1 gallon plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cosmo's Food Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
Edwards Lifesciences Rigid Suction Wand, sterile. Model numbers S033 and SPC2081. Product Usage: These suction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jul 18, 2012
IntelliSpace Portal software and Extended Brillance Workspace software Intellispace Portal is a multimodality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2012
Tom's Bacon Cheddar Fries, Flavored Corn and Potato Snacks, Net Wt., 2.75 oz (78.0g),
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snyder's - Lance Inc.
FDA (openFDA food enforcement)
Reported Jul 18, 2012
superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.superDimension, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2012
TDX SP Power Wheelchair, TDX SR Power Wheelchair, TDX SI Power Wheelchair. Model Number(s): TDXSI, TDXSI-2, TDXSI-2-S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jul 11, 2012
Microbiologics 217 Osseo Avenue North, St. Cloud, MN 56303, Gram Stain Control Slides, SLO3-10, ATCC Licensed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Jul 4, 2012
ARCHITECT CA 19-9XR Reagent Kit; ARCHITECT CA 19-9 Reagent Kit, list 291-20 (4 x 100 tests), 2K91-25 and 2K91-27 (1 x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jul 4, 2012
CJ Het Oyster (CJ Frozen Oyster), 40x8oz.. Material#912329, Frozen Oyster (KR 12 SP 050110), Material#912330, Frozen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CJ Foods, Inc., A Division
FDA (openFDA food enforcement)
Reported Jul 4, 2012
Hartmann Econolux Ref 416 105 Sterile Gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges For use in wound…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hartmann USA, Inc.
1 more product 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.