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 Dec 18, 2019
Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers
FDA (openFDA food enforcement)
Reported Dec 11, 2019
PANTERA Proximal Humerus Fracture Plate System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toby Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2019
3021 BROCCOLI FLORETS 3LB; 3026 BROCCOLI DICED 5LB; 3029 BROCCOLI FLORETS 4/3#; 3023 BROCCOLI STIR FRY CUT 4/3# all…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vinyard Fruit & Vegetable Co., Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 4, 2019
Alinity ci Level Sensor, Bulk Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Nut Bread Net Wt. 16 oz (454 g), Maufactured by Beatrice Bakery Co, Beatrice, NE.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beatrice Bakery Co.
FDA (openFDA food enforcement)
Reported Dec 4, 2019
Atellica CH 930 Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Great Value Old Fashioned Glazed Donuts packaged in a paperboard box with cellophane window and each box contains 6…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.United States Bakery Corp.
FDA (openFDA food enforcement)
Reported Dec 4, 2019
ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2019
EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Neocis Guidance System Fiducial Array - Product Usage: The Neocis Guidance System (NGS) is a computerized navigational…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neocis Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2019
The PolarCath Balloon Catheter consists of a coaxial catheter shaft with two concentric, non-compliant balloon systems…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nucryo Vascular Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2019
TEMPLE PURE PRANA MATCHA+SHOT; 3 FL OZ (89mL); VITALITY SUPERBOOST; COLD PRESSURED; PERISHABLE KEEP REFRIGERATED;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Temple Turmeric Inc.
FDA (openFDA food enforcement)
Reported Nov 20, 2019
Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cadence Science, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Visual-ICE Cryoablation System, FPRCH6000. The cryoablation system is a mobile console system intended for cryoablative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galil Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
2000 Vascular with 30 Degree option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2019
MODIFIED INSTRUMENTS: Trial Spacer 7mm with T-Handle Trial Spacer 8mm with T-Handle Trial Spacer 9mm with T-Handle…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 6, 2019
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Nov 6, 2019
SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk GmbH
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Simmons Prepared Foods, Inc. Retira Productos De Aves Debido A Una Posible Contaminación Con Materia Extraña
High riskUsing this product could cause serious injury, illness or death — stop using it now.Simmons Prepared Foods, Inc.
USDA FSIS
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 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.