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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.

Medical devices

Reported Feb 24, 2021

IOLMaster 700

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

Carl Zeiss Meditec AG

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral…

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

Confirm Biosciences Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biopsy Needle, 1/7F…

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

Argon Medical Devices, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed…

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

Arjohuntleigh Magog, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

PRYTIME MEDICAL REBOA Catheter Introducer Kit, REF: KT1835C, Contents: Needle, 18 GA x 7 CM ECHOGENIC, STERILE, 1 EA,…

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

Prytime Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2021

FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 10, 2021

RUFFLES "PARTY SIZE" ORIGINAL POTATO CHIPS 13 1/2 oz. UPC 028400034005 packaged in flexible bags

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

Frito-Lay, Inc. Headquarters

FDA (openFDA food enforcement)

Food

Reported Feb 3, 2021

Blueberry Blizzard Coffee Cake, Item 259, Net Wt. 24 oz.

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

Nueske Applewood Smoked Meat, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 3, 2021

O H Danish Bakery Almond Danish Kringle, UPC 67209-00006. Net Weight: 24 oz. (1 lb. 8 oz) 680.3 grams

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

O & H Danish Bakery

FDA (openFDA food enforcement)

Medical devices

Reported Feb 3, 2021

Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…

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

Respironics California, LLC

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2021

Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…

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

Penumbra Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 27, 2021

FITNESS LABS***Organic***Coconut Oil***Extra Virgin***16 fl. oz. (473 mL)***Carefully Designed and Distributed by…

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

Piping Rock Health Products

FDA (openFDA food enforcement)

Medical devices

Reported Jan 20, 2021

Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF…

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

Boston Scientific Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended for patients for whom the monitoring of…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

VITROS Chemistry Products TP Slides- IVD measure total protein (TP) concentration in serum and plasma using VITROS…

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

Ortho Clinical Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…

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

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 13, 2021

9" French Silk Base, Item 7545, Count per case 6 Ea., Case Weight 12 lb. 3 oz. UPC 50796220075458. Keep Frozen.

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

American Blue Ribbon Holdings LLC

FDA (openFDA food enforcement)

Food

Reported Jan 13, 2021

Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing Millersburg, OH 44654.

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

Lipari Foods Operating Company, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 30, 2020

Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…

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

Cook Inc.

20 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 30, 2020

CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ (396g) Canyon Bakehouse, LLC Johnstown, CO 80534 UPC 8…

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

Flowers Foods (Corporate Offices)

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 30, 2020

Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…

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

ICU Medical, Inc.

12 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.