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.
2,558 stored notices name Arkansas, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.
Reported Jul 13, 2022
Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
ABL800 Flex Analyzer Model Numbers 393-800 and 393-801
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Dimension LTNI -In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2022
VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2022
Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Volcano Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 29, 2022
Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 29, 2022
Mini Peanut Butter Cream Pie. Product was available for purchase at the following banner: Haggen. Packaged in clear…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Albertsons Companies LLC
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 29, 2022
Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Farms Retail Inc.
FDA (openFDA food enforcement)
Reported Jun 22, 2022
illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 22, 2022
Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2022
SUPPLE BEARS QUERCETIN BROMELAIN GUMMIES + Vitamin C & Zinc 60 DIETARY SUPPLEMENTS NO SOY, NO GLUTEN, NO EGGS, NO…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.6174 Industries, LLC
FDA (openFDA food enforcement)
Reported Jun 15, 2022
yellow flesh bulk peaches product of Chile bulk approximately 16lbs. per case PLU 4044
High riskUsing this product could cause serious injury, illness or death — stop using it now.Brookshire Grocery Co.
FDA (openFDA food enforcement)
Reported Jun 15, 2022
Back up batteries in Ventilators labeled as the following: a. CARESCAPE R860 Ventilators (K142679) b. ENGSTROM…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2022
STORZ KARL STORZ-ENDOSKOPE REF 11272VUE CMOS Video Cysto-Urethroscope REF 11272VUEK CMOS Video Cysto-Urethroscope…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jun 15, 2022
Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.
High riskUsing this product could cause serious injury, illness or death — stop using it now.The TJX Companies, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2022
Resin UPDATE CD-ROM, REF: 250-3020 inside VARIANTnbs Sickle Cell Program Reorder Pack, REF: 250-3000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2022
The C304-HIS device features a guide wire to access the vein, a valve to reduce blood loss during the implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jun 8, 2022
JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The JM Smucker Company LLC
23 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 1, 2022
Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
AC-powered adjustable medical beds with built-in electric DC actuators and controls.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Umano Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Vascular
FDA (openFDA device enforcement)
Reported May 25, 2022
MicroScan WalkAway-40 plus Instrument REF B1018-283
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 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.