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 48,784 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.
Reported May 4, 2016
Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Self-Cath¿ Pediatric Catheter Size CH 06, Product # 5044101400, Catakig # 306. Product Usage: The Self-Cath…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Apr 27, 2016
GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materne North America Corp.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 27, 2016
GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle Infant Nutrition
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 27, 2016
iVue and iVue 500 (now called iScan) OCT systems with software version 2016.0.0.127 (USA only) and 2016.1.0.127 (out of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arjo, Inc. dba ArjoHuntleigh
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Arthrex Deltoid Ligament Reconstruction Implant System. Intended as a fixation post, a distribution bridge or for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Bumble Bee Chunk Light Tuna in Water, 48cans/case, 5oz, UPC 8660000020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bumble Bee Foods LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 20, 2016
GE Healthcare, Aisys CS2 anesthesia..
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Brilliance 64:Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endovascular
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Gomco Style Circumcision Clamp Trays is an instrument used to compress the foreskin of the penis during circumcision of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Country Life Natural Foods Labeled SHELLED PISTACHIOS RAW NET WT. 2lb (906 g) plastic bags item 030244 and Batch 1357…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oak Haven, Inc. dba Country Life Natural Foods.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
Chef Hon brand STEAMED BUNS WITH SEAFOOD & VEGETABLE, Net Wt. 1 lb. 8 oz. (682g), UPC 7 47518 00156 2, Product Code #…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peking Food LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
Sweetwater Sprouts 100% Pure Sprouted Alfalfa packaged in the following configurations: 4 oz. plastic bags (UPC 7 56733…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sweetwater Farms LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 13, 2016
Guardian II Hemostasis Valve, models 8210 and 8211. The following models are only available Outside the US: FH101,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Favorites Natural Pistachios, roasted & salted, 4.5 oz (128g) pouch UPC 0 38445 12286 5 Proudly distributed by Circle K…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kanan Enterprises, Inc.
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pelton & Crane / Marus / DCI Equipment / KaVo
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Prosupps Dr. Jekyll INTENSE PUMP PRE WORKOUT, 30 SERVINGS, WATERMELON NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSupps USA LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Cios Alpha, mobile X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
15 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.