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 Nov 26, 2025
PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 19, 2025
Peach Salsa; UPC 85006540364 14oz (397g); Use by 10/12/2025 to 10/29/2025
High riskUsing this product could cause serious injury, illness or death — stop using it now.GBC Food Services, LLC
FDA (openFDA food enforcement)
Reported Nov 19, 2025
Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, LP
20 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 19, 2025
Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Corporation Medical Systems Division
FDA (openFDA device enforcement)
Reported Nov 12, 2025
SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent, REF: 969706
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2025
Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage Stereotactic System Software Version: n/a Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2025
Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ice Cream Factory, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 12, 2025
Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2025
CellMek SPS Sample Preparation System, REF: C44603. Software versions 2.2.122.0 and prior, and Instructions for Use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA Nasal Complete kit; 10 test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Nov 5, 2025
ChemoLock Bag Spike, 01 units REF: CL-10-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
37 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Thermo scientific MAS Omni CARDIO, Liquid Assayed Integrated Cardiac Control, Model/Catalog Number: OCRD-L, OCRD-101,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Model: Incisive CT; Product Code (REF): (1) 728143, (2) 728144; Software Versions: 5.1.0.X & 5.1.1.X;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2025
READY MEALS Pesto Bowtie Pasta Salad, UPC 27133 #####. Product was made in-store with store generated scale label…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Albertsons Companies LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 29, 2025
Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2025
Artegraft¿ Collagen Vascular Graft; REF: AG1015;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
FDA (openFDA device enforcement)
Reported Oct 29, 2025
LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2025
Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 22, 2025
CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
15 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Free Range Grade A Large Brown Eggs, 12ct Cartons, UPC: 860010568507, Black Sheep Egg Company 400 S Memorial Drive…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Black Sheep Egg Company, LLC
9 more products in this recall
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new Arkansas recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.