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.

2,558 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.

Medical devices

Reported Dec 25, 2024

Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the…

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

Spacelabs Healthcare, Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2024

Baker Farms CURLY MUSTARD 16 oz NET WT 16 oz UPC 8 13098 02018 4 Baker Farms 3667 Ellenton-Norman Park Road Norman…

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

Terry and Joe Baker Farms, LLC dba Baker Farms

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

"***SUPER***BRAND***DRIED CINNAMON POWDER***Net Wt: 4oz(113g)***PRODUCT OF CHINA***DISTRIBUTOR: IHA BEVERAGE COMMERCE,…

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

Kim-Seng Company

FDA (openFDA food enforcement)

Food

Reported Dec 18, 2024

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

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

Tipp Distributors, Inc. dba Novamex

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2024

(1) READY MEALS GREEN CHILI CHICKEN ENCHILADAS SS COLD (UPC 21291600000) (2) GREEN CHICKEN ENCHILADAS 6 CT SS COLD (UPC…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)

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

Cartiva, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2024

AROMA VITA HOT COCOA MIX, NET WT. 32OZ (2LBS) 907g, UPC 7 1908 50007 0, Case UPC 50719098500075, Distributed by DYMA…

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

Dyma Brands

20 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2024

Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Abbott Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…

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

Kci USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL

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

Shimadzu Corp. Analytical & Measuring Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product…

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

Olympus Corporation of the Americas

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B,…

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

Philips Respironics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 20, 2024

Home Chef Chicken Street Taco, Net Wt. 9.93 oz, packaged in a plastic tray with clear plastic lid, perishable item kept…

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2024

Cartesion Prime, Digital PET-CT, Model: PCD-1000A/3D.004, PCD-1000A/3D, is a diagnostic imaging system that combines…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2024

Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number:…

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

Hammond's Candies Since 1920 II, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2024

SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and fluoroscopic…

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

Shimadzu Corporation Medical Systems Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Home Alone International Delight Peppermint Mocha Zero Sugar, 32oz plastic bottle, 6 bottles per case. Refrigerated.

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

Danone US LLC

FDA (openFDA food 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.