Recalls distributed in Arkansas
These notices name Arkansas 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.
2,595 stored notices name Arkansas, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.
Reported May 7, 2014
Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altasource LLC dba Meta Labs LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
VITROS Chemistry Products CDM PROM (Calibration Data Module) No. 0168, Catalog Number/REF 199 9077, used in conjunction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Apr 23, 2014
SmartSite Extension Set, Model No. 20029E, intravascular administration set.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Apr 23, 2014
Luna Chocolate Chunk; Whole Nutrition Bar for Women; 15 count box. Clif Bar & Company, Emeryville, CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clif Bar And Company
FDA (openFDA food enforcement)
Reported Apr 16, 2014
7mm Drain Kit, Flat Full Perforated, Saber 100ml Bulb and 3C System Sterile (10/case) Intended for closed wound suction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aspen Surgical Products, Inc.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 16, 2014
Prego Italian Sauce Traditional, NET WT. 24 OZ (1 LB. 80 Z.)(680 g) in glass jars.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Campbell Soup Supply Co., LLC
FDA (openFDA food enforcement)
Reported Apr 16, 2014
Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Ideal Protein Double Chocolate Brownie. Individually wrapped, sold in boxes of 7.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Laboratories Cop Inc.
FDA (openFDA food enforcement)
Reported Apr 9, 2014
Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland), Inc.
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Artis Zee Angiographic x-ray systems.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Weck Vista Universal Laparoscopic Port, Size 5/10mm x 100mm, Catalog No. 405910, Weck Vista Universal Laparoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2014
Missouri Firm Recalls Chicken Nugget Products Due To Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tyson Foods, Inc.
USDA FSIS
Reported Apr 2, 2014
Bonduelle USA Inc (Oakfield) BEANS GREEN CUT GRADED, Net weight: 1,480 lbs (bulk form in Totes), Keep frozen.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bonduelle USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 2, 2014
Drill Template and the Saw Guide for the Ulna Osteotomy System. Intended for fixation of fractures, osteotomies,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Apr 2, 2014
HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2014
Oklahoma Firm Recalls Chicken Products Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.AdvancePierre Foods, Inc.
USDA FSIS
Reported Mar 26, 2014
Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens, FL 33410 USA 1-800-342-5454***EDAZ , EDAZx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2014
syngo Dynamics Picture Archiving and Communication System (PACS). Model numbers 10091804, 10091805, 10091806, 10091807,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 PAT N-K FLEX MBACK SZ 1 PAT N-K FLEX MBACK SZ 2 PAT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Jalapeno Ground 40, Elite Spice Code #JP9520, 50 lb poly-lined cartons labeled in part ***Elite Spice Inc. 7151…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elite Spice Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 19, 2014
GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 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.