The Recall Desk

State

Arkansas product recalls

72,992 recalls have nationwide distribution and so reach Arkansas. 5,513 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total
5,513
Critical
1,018
Severe
1,210
Most recent
2026-09-09

Of the 5,513 recalls naming Arkansas we have scored against our rubric, 1,018 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,210 (22%) are Severe.

These figures cover only the 5,513 recalls whose distribution notice names Arkansas specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7326–7350 of 78505

  • HighCPSC·25206·2025-04-03

    HONEYJOY High Chairs Recalled for Suffocation Risk from Incline Violation

    HONEYJOY Convertible and Foldable High Chairs are being recalled because they were marketed for infant sleep with an incline angle exceeding 10 degrees, violating federal safety regulations. About 2,750 units sold exclusively on Amazon from April 2023 to August 2024 are affected.

    Product
    HONEYJOY Convertible and Foldable High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25214·2025-04-03

    Vivitar Blender Bottles Recalled by Sakar for Laceration Hazard

    Sakar International is recalling about 199,000 Vivitar Blender Bottles sold at Target because the blades can continue operating when the bottle is removed from the base. No injuries have been reported.

    Product
    Vivitar Blender Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25203·2025-04-03

    DEWALT 70,000 BTU Outdoor Propane Heaters Recalled for Fire and Burn Hazards

    About 21,250 DEWALT 70,000 BTU outdoor propane heaters are being recalled due to operating instructions that can prevent proper fan operation, causing overheating and fire and burn hazards. No injuries have been reported.

    Product
    DEWALT 70,000 BTU Outdoor Portable Cordless Forced Air Propane Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25209·2025-04-03

    Foldable Travel Hair Dryers Recalled Due to Electrocution and Shock Hazards

    AliExpress is recalling about 80 foldable travel hair dryers sold from April 2022 through January 2025 because they lack immersion protection and can cause electrocution or shock if they fall into water while plugged in. No injuries have been reported.

    Product
    Foldable Travel Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V184000·2025-04-03

    Nova Bus LFS Transit Buses Recalled for Battery Fire Risk

    Nova Bus is recalling 2022-2023 LFS transit buses because high voltage battery hardware may come loose and cause a short circuit, creating a fire risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25211·2025-04-03

    LVOE Hair Dryers Recalled for Electrocution and Shock Hazards

    AliExpress is recalling LVOE-brand hair dryers sold from April 2023 through December 2024 because they lack immersion protection and can cause electrocution if they fall into water while plugged in. No injuries have been reported.

    Product
    LVOE Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25210·2025-04-03

    Mini travel hair dryers recalled for electrocution and shock hazard

    XZT mini hair dryers sold on AliExpress lack immersion protection and can cause electrocution or shock if they fall into water while plugged in. No injuries have been reported.

    Product
    Mini Travel Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0300-2025·2025-04-02

    SinuCleanse Nasal Saline Packets Recalled for Bacterial Contamination

    SinuCleanse Premixed Saline Packets sold nationwide are being recalled due to contamination with Staphylococcus aureus, a bacterium that can cause infection.

    Product
    SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg) for Nasal Wash System, 60-count All Natural USP Grade Saline Packets, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00103 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·010-2025·2025-04-02

    Hearthside Recalls Breakfast Sandwiches for Undeclared Sesame Allergen

    Hearthside Food Solutions is recalling approximately 489,887 pounds of ready-to-eat breakfast sandwiches because they contain sesame, a known allergen, that is not declared on the label.

    Product
    Hearthside Food Solutions LLC d/b/a Maker's Pride — Hearthside Food Solutions, LLC Recalls Ready-To-Eat Sausage and Bacon Breakfast Sandwiches Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0299-2025·2025-04-02

    SinuCleanse Nasal Wash System Recalled for Bacterial Contamination

    Ascent Consumer Products Inc. is recalling SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System nationwide due to bacterial contamination with Staphylococcus aureus. Affected lot number is 024122661Al with expiration date 12/2027.

    Product
    SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 Soft tip Squeeze Bottle, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V205000·2025-04-02

    Jayco Recalls 2024-2025 Entegra Motorhomes Due to Fuel Hose Separation

    Jayco is recalling 2024-2025 Entegra Anthem, Aspire, and 2025 Reatta XL motorhomes because a fuel hose may separate, causing a leak, fire, or engine stall.

    Product
    ENTEGRA — ENTEGRA ANTHEM, ASPIRE, REATTA XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1396-2025·2025-04-02

    CVAC Aspiration System Requires Labeling Update for Pressure Risk

    The CVAC Aspiration System requires a labeling update to add safety instructions for high-viscosity kidney fluid. Continuing fluid inflow without adequate outflow can create dangerous intrarenal pressure imbalances.

    Product
    CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of urinary tract and kidney interior.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0301-2025·2025-04-02

    SinuCleanse Neti Pot Nasal Wash System Recalled for Bacterial Contamination

    Ascent Consumer Products Inc. is recalling SinuCleanse Soft Tip Neti Pot Nasal Wash System due to bacterial contamination with Staphylococcus aureus. Consumers should stop using this product immediately.

    Product
    SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 kettle style Neti Pot, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1441-2025·2025-04-02

    Medline Surgical Procedure Kits Recalled for Syringe Leakage and Breakage

    Medline Industries has recalled 11,774 surgical procedure kits with defective plastic syringes that may leak or break. The kits were distributed nationwide and in Canada.

    Product
    Medline procedure kits labeled as: 1) ABLATION PACK, Pack Number DYNJ40629B; 2) ACH LAPAROSCOPIC GB PACK, Pack Number DYNJ67756A; 3) CHRISTUS WH LAP CHOLE PACK, Pack Number DYNJ60934B 4) CRMC LAP CHOLE DIAG LAP-LF, Pack Number DYNJ61095D; 5) CYSTO PACK, Pack Number DYNJ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1418-2025·2025-04-02

    Baxter TruSystem 7500 Hybrid: Software Issue Disables Back Adjustment

    Baxter is recalling the TruSystem 7500 Hybrid due to a software issue that prevents the upper back section from being adjustable when emergency mode is enabled.

    Product
    Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1430-2025·2025-04-02

    Pressure Monitoring Lines Recalled for Manufacturing Defect in Luer Fittings

    Medline Industries is recalling namic medical convenience kits containing Pressure Monitoring Lines with defective female luer fittings manufactured with excess material. The defect could impair device function.

    Product
    namic convenience kits labeled as: MTS,COLOR,PML,KIT,-,FRENCH HOSPITAL PG; medical convenience kit, REF 600605710
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0296-2025·2025-04-02

    Compounded Fentanyl-Bupivacaine Epidural Injections Recalled for Sterility Failure

    QuVa Pharma recalls compounded fentanyl-bupivacaine epidural injections due to lack of assurance of sterility. The recall affects 2,310 cassettes distributed nationwide.

    Product
    fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1448-2025·2025-04-02

    Medline C-section procedure kits recalled for syringe quality defects

    Medline is recalling C-section procedure kits because plastic syringes in the kits may leak or break. The defect was identified in connection with an FDA safety alert and poses a potential risk to patient health.

    Product
    Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ57622; 2) C SECTION PACK, Pack Number DYNJ48483B; 3) C SECTION PACK, Pack Number DYNJ61573; 4) C SECTION PACK, Pack Number DYNJ66801; 5) C SECTION PACK-LF, Pack Number DYNJ0367951P; 6) C SECTION PACK-LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0298-2025·2025-04-02

    Babyganics Mineral Sunscreen Recalled for Failed Stability Specifications

    Babyganics Sheer Blend SPF 50 Mineral Sunscreen is being recalled nationwide because ingredients separated during stability testing, prompting an FDA Class II recall.

    Product
    babyganics, Sheer Blend, SPF 50 Mineral Sunscreen Fragrance Free (zinc oxide 20%), a) 1.7 FL OZ (50 mL) bottle, UPC 810035921658, b) 8 FL OZ (236 mL) bottle, UPC 810035921382, Dist. by KAS Direct, LLC, 1525 Howe St., Racine, WI 53403, Made in Canada.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1465-2025·2025-04-02

    Medline procedure kits with defective plastic syringes recalled due to leak and breakage risk

    Medline procedure kits containing plastic syringes are being recalled due to leaks, breakage, and quality issues that may compromise sterile medical procedures. Approximately 14,589 units were distributed nationwide in the US and Canada.

    Product
    Medline procedure kits labeled as: 1) ACL ARTHROSCOPY PACK, Pack Number DYNJ55316G; 2) ARTERIOGRAM PACK, Pack Number DYNJ64332; 3) ARTHRO PACK-LF, Pack Number DYNJ38748F; 4) ARTHRO PACK-LF, Pack Number DYNJ38748F; 5) ARTHROGRAM PACK, Pack Number DYNJ65817; 6) ARTHROGRAM TR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1415-2025·2025-04-02

    Baxter Floor Mounting Column TS 7500 U Software Issue Affects Emergency Function

    Baxter is recalling 33 units of the Floor Mounting Column TS 7500 U due to a software defect that prevents upper back adjustment when emergency mode is enabled.

    Product
    Baxter Floor mounting column TS 7500 U, Product Code 1730732
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1466-2025·2025-04-02

    Checkpoint Guardian Intraoperative Lead adhesive defect electrical leakage risk

    The adhesive on Checkpoint Guardian Intraoperative Leads may not fully cover metallic wire components, leading to potential electrical current leakage. This could result in inconsistent muscle responses and affect surgical effectiveness.

    Product
    Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraoperative Lead, Small Model/Catalog Number: REF# 9524 (Small) Product Description: The Checkpoint Guardian Intraoperative Leads are single-patient disposable accessories for providing s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1408-2025·2025-04-02

    Premier Solo Diamond dental burs recalled due to material hardness defect

    Premier Dental Products Co is recalling Premier Solo Diamond Large dental burs because the material hardness does not meet specifications and may cause the burs to bend during use. 77 units in six U.S. states are affected.

    Product
    Premier Solo Diamond - Large Invented Cone; SKU: 807016C.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0292-2025·2025-04-02

    Metformin Hydrochloride Extended-Release Tablets Recalled for Foreign Tablet Contamination

    A-S Medication Solutions is recalling 411 bottles of Metformin Hydrochloride Extended-Release 500mg tablets (Lot #4260340) distributed nationwide due to the presence of foreign tablets or capsules.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide