All recall categories

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.

2,592 stored notices name Arkansas, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Arkansas too — those are in the archive.

Food

Reported May 26, 2021

ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hi Tech Pharmaceuticals

13 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 26, 2021

Newly Weds A70088 bread crumbs X1, 35lbs bag

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Newly Weds Foods Inc.

21 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 26, 2021

PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Public Goods

FDA (openFDA food enforcement)

Medical devices

Reported May 26, 2021

Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard includes suction with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

WillowWood Global LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 19, 2021

PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 19, 2021

ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL Assurity and Endurity pacemakers are intended to…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

St. Jude Medical, Cardian Rhythm Management Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 19, 2021

Hershey s Chocolate Shell Topping plastic bottles in cases labelled Heath Shell Topping, 7.25 oz., 6 bottles per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Hershey Company

FDA (openFDA food enforcement)

Medical devices

Reported May 12, 2021

Centricity Universal Viewer - Product Usage: intended to assist in the viewing, analysis, diagnostic interpretation,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 12, 2021

VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Food

Reported May 12, 2021

Jule's Cashew Brie (Classic) Net Wt. 6 oz. (1.70g) Keep Refrigerated. UPC 860388001507

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Jule's Foods

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 12, 2021

Grace Medical REF S-2500 *** SHEEHY BONE DUST COLLECTOR *** Stainless steel filter - Product Usage: intended to be…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Oto Med Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 5, 2021

Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 5, 2021

Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medela AG Medical Technology

FDA (openFDA device enforcement)

Medical devices

Reported May 5, 2021

Power Wheelchair

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merits Holdings Co. dba Merits Health Products, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 5, 2021

VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported May 5, 2021

Tuscan Garden Ranch Dressing, packaged in 16 oz bottles, Dist. & Sold Exclusively by ALDI, Batavia, IL packaged in 12…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Richelieu Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported May 5, 2021

Dark Chocolate Expresso Beans; Net Wt. 12 oz. (340g), Best if used by 11-19-2021. Contains Soy, May Contain Milk.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Torn & Glasser, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 28, 2021

Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Angiodynamics Inc. (Navilyst Medical Inc.)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 28, 2021

The AMS 700 Inflatable Penile Prosthesis is a closed fluid-filled system containing saline. The system is made out of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Apr 28, 2021

Freshness Guaranteed Macaroni Salad Amish, item # 579284, refrigerated, packaged in a clear cup with clear snap on lid,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Reser's Fine Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 28, 2021

BCS XP System: Multipurpose system for in vitro coagulation studies. Product code: 10459330, 10461894, 10470625 -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 28, 2021

Trader Joe's Restaurant Style White Corn Tortilla Chips; Net Wt. 9 oz. (255g)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Snak King Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Apr 21, 2021

MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is then…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 21, 2021

Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For use with Signia stapling system. Staple…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien LLC

FDA (openFDA device enforcement)

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Other states

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.