The Recall Desk

State

Arkansas product recalls

20,304 recalls have nationwide distribution and so reach Arkansas. 0 additional recalls listed Arkansas specifically in their distribution scope.

About recalls in Arkansas

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Arkansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11201–11225 of 20304

  • HighFDA (Devices)·Z-0316-2024·2023-11-22

    Ocean Chest Drains Recalled for Inadequate Assembly Instructions

    Atrium Medical recalls Ocean chest drains due to insufficient precaution instructions for proper catheter and tube connection setup. Improper assembly could compromise device function.

    Product
    Ocean Water Seal Chest Drains (Ocean): Products REF Number Product Name (1)2002-000 DRAIN, OCEAN SINGLE W/AC,S; (2)2002-040 DRAIN, OCEAN SINGLE,PEDI CONNECTOR; (3)2002-100 DRAIN, OCEAN SINGLE W/AC; (4)2002-300 DRAIN, OCEAN SINGLE W/S; (5) 2002-400 DRAIN, OCEAN SINGLE ;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24031·2023-11-22

    Lenovo USB-C Laptop Power Banks Recalled for Fire Hazard

    Lenovo is recalling about 2,850 USB-C laptop power banks because internal screws can loosen, causing a short circuit and lithium-ion battery overheating. One fire with minimal property damage has been reported.

    Product
    Lenovo USB-C Laptop Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0301-2024·2023-11-22

    LIFEPAK 15 Defibrillator Recalled for Loose Battery Pins Causing Power Loss

    Physio-Control is recalling LIFEPAK 15 defibrillators due to potential loose battery pins that could cause power failure. Four affected units have been distributed to Arizona, California, North Carolina, New Jersey, and New York.

    Product
    LIFEPAK 15, REF: 99577-001955, Part Number V15-5-000584 and V15-7-000020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0419-2024·2023-11-22

    Amazon Fresh Frosted Mini Brownies recalled for potential plastic contamination

    Amazon Fresh Frosted Mini Brownies (Item 19858) may contain plastic pieces. The 12-count packs distributed nationwide are subject to recall.

    Product
    Item 19858, Amazon Fresh, Frosted Mini Brownie with yellow and purple icing with sprinkles, 12 count per pack, packaged in a plastic clear clamshell container, net wt. 14oz. Case UPC 1 08 42379 19858 5; Retail package UPC 8 42379 19858 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0292-2024·2023-11-22

    Philips Big Bore RT CT Scanner Defect May Cause Incorrect Treatment Planning

    A software defect in Philips Big Bore RT CT scanners may cause incorrect coordinates in radiation therapy planning systems, affecting 56 units distributed nationwide and internationally.

    Product
    Big Bore RT with software version V4.8.0.10421- Model: 728242 CT scanner and simulator designed for radiation oncology and therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0304-2024·2023-11-22

    LIFEPAK 15 Defibrillators Recalled Due to Potential Loose Battery Pins

    Physio-Control has recalled LIFEPAK 15 defibrillators because battery pins may become loose, causing power issues. Owners should contact the manufacturer for instructions on how to proceed.

    Product
    LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0308-2024·2023-11-22

    Laboratory Culture Disks Recalled for Aspergillus Flavus Contamination

    Microbiologics Inc is recalling LYFO-DISK P. venetum laboratory culture disks (lot 794-142) found contaminated with Aspergillus flavus during complaint investigation. The product was distributed worldwide.

    Product
    LYFO-DISK, P. venetum, Catalog number 0794L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0319-2024·2023-11-22

    CT Scanner Software Bug May Cause Gantry to Move to Wrong Position

    Philips Spectral CT on Rails software version 5.1.0 may fail to move the needle position to the desired location during scans. This could cause the gantry to move unexpectedly and potentially collide with the user or needle.

    Product
    Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0318-2024·2023-11-22

    Express Dry Seal Chest Drains Recalled for Insufficient Setup Instructions

    Atrium Medical Corporation is recalling Express Dry Seal Chest Drains (models 4000-100N and 4050-100N) due to inadequate instructions for proper catheter and patient tube connection setup. No injuries have been reported.

    Product
    Express Dry Seal Chest Drains (Express): 4000-100N DRAIN, EXPRESS, SINGLE; 4050-100N DRAIN, EXPRESS, BRU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0294-2024·2023-11-22

    CT Scanner Image Fusion Software Error Affecting Radiation Therapy Planning

    A software bug in Philips Brilliance CT scanners causes image-fusion errors, resulting in incorrect radiation therapy coordinates and potential treatment planning failures.

    Product
    Brilliance CT Big Bore Oncology with software version V4.8.0.10421 Model:728243 CT scanner and simulator designed for radiation oncology and therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0295-2024·2023-11-22

    IBA Proton Therapy System Patient Positioning Can Move Unexpectedly

    The IBA Proton Therapy System's patient positioning system can perform unexpected motions, risking patient crushing. Five US units and nine international units are affected.

    Product
    IBA Proton Therapy System - PROTEUS 235. PTS-11 versions, PTS-12 versions with Orion PPS version OSS6.0. Configured with Orion Patient Positioning System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·24030·2023-11-22

    Balloon Time Mini Helium Tanks Recalled Due to Projectile Injury Risk

    Approximately 121,100 Balloon Time Mini Helium Tanks are being recalled because compressed helium can escape and cause the plastic cap to be ejected, potentially striking users or bystanders. No injuries have been reported.

    Product
    Balloon Time Mini Helium Tanks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0223-2024·2023-11-22

    Siemens Mobilett Mira wireless x-ray systems recalled for buzzer mounting defect

    Four Siemens Mobilett Mira wireless mobile x-ray systems are recalled due to incorrect buzzer component mounting that prevents acoustic signals during x-ray activation. The systems remain fully functional with visual LED indicators available for operator monitoring.

    Product
    Mobilett Mira wireless (VA20) mobile x-ray system(s)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·24028·2023-11-21

    ZLINE RG Gas Ranges Recalled for Carbon Monoxide Hazard

    ZLINE is recalling about 30,000 RG gas ranges (30-inch, 36-inch, and 48-inch models) because the oven can emit dangerous levels of carbon monoxide, posing a serious risk of injury or death.

    Product
    ZLINE 30-inch, 36-inch and 48-inch RG gas ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24026·2023-11-16

    Tractor Supply Red Shed Hammock Swing Chairs Recalled Due to Fall Hazard

    Tractor Supply is recalling about 7,500 Red Shed® Hammock Swing Chairs because the plastic buckle supporting the back can break while someone is seated, causing a fall. The company has received 13 reports of buckle or stitching failures, including three falls.

    Product
    Red Shed® Hammock Swing Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24715·2023-11-16

    Target Recalls Hearth & Hand Toy Mushroom Peg Sorters Due to Choking Hazard

    Target is recalling about 1,850 units of its 13-Piece Toy Mushroom Peg Sorters because the mushroom stems can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    13-Piece Toy Mushroom Peg Sorters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24714·2023-11-16

    LAOION Children's Cups Recalled for Lead Content and Lid Hazards

    LAOION children's cups sold on Amazon contain lead in solder on the cup bottom and have lids that can crack, creating choking and laceration risks. About 200 units were sold from March to May 2023.

    Product
    LAOION Children's Cups
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24027·2023-11-16

    Khaite Women's High Heeled Sandals Recalled for Detaching Heels and Fall Risk

    Khaite is recalling approximately 1,860 women's high heeled sandals from its Spring Summer 2024 collection because the heels can detach, creating a fall hazard. Consumers should stop using the shoes immediately and contact Khaite for a refund.

    Product
    Women's high heeled sandals (Spring Summer 2024 collection, Louisa, Linden and Seigel Heel Sandals)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0101-2024·2023-11-15

    Lidocaine injection recalled due to glass particulate matter

    Pfizer Inc. is recalling 21,390 vials of Lidocaine Hydrochloride 1% injection due to presence of glass particulate matter. Lot 42290DK with expiration 6/1/2024 is affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0184-2024·2023-11-15

    Alaris PCA Module 8120 infusion pump recalled for unvalidated syringes

    CareFusion 303, Inc. is recalling the Alaris PCA Module 8120 infusion pump because its labeling lists compatible syringes that have not been validated. This Class I recall affects 867,362 units worldwide.

    Product
    BD Alaris PCU REF 8015
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0193-2024·2023-11-15

    Olympus Bronchovideoscope Recalled Due to Combustion Risk

    Olympus is recalling 719 EVIS EXERA b Bronchovideoscope Model BF-XT190 devices due to risk of endobronchial combustion during high-frequency cauterization when oxygen is supplied or the electrode is too close to the device tip.

    Product
    EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-XT190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0192-2024·2023-11-15

    Olympus Bronchovideoscopes Recalled for Endobronchial Combustion Risk

    Olympus is recalling bronchovideoscopes nationwide due to a risk of combustion inside the bronchial passages during high-frequency cauterization if oxygen is supplied or the electrode is positioned too close to the scope's tip.

    Product
    EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190, BF-H190, BF-Q190 and BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 Model Number BF-Q170
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0189-2024·2023-11-15

    Five Olympus Bronchovideoscope Models Recalled for Endobronchial Combustion Risk

    Olympus is recalling 15,942 bronchovideoscope units nationwide due to endobronchial combustion risk during cauterization procedures with oxygen supply. The hazard occurs when the electrode of the surgical accessory is positioned too close to the scope's distal end.

    Product
    BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T150, BF-1T60, BF-P150 BF-P60 and EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Number XT160
    Category
    Medical Device
    Distribution
    Distributed nationwide