The Recall Desk

State

Delaware product recalls

20,188 recalls have nationwide distribution and so reach Delaware. 0 additional recalls listed Delaware specifically in their distribution scope.

About recalls in Delaware

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 Delaware 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.

8051–8075 of 20188

  • HighFDA (Devices)·Z-2572-2024·2024-08-21

    Merit Medical Convenience Kits with Defective Syringes Recalled

    Merit Medical convenience kits containing defective syringes are being recalled for leaks and breakage that may pose a risk to patient health.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude Prestige (Introducer Catheter), REF: PLP-2505/A PLP-2514/A PLP-2516/A The introduction of various types of pacing/defibrillator leads and catheters i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2557-2024·2024-08-21

    Merit Medical convenience kits recalled for syringe leaks and breakage

    Merit Medical convenience kits containing recalled syringes have quality issues including leaks and breakage that may pose a risk to patient health. The recall affects 2,388 kits distributed nationwide.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid Response Waste Management System Kit, REF BRC-BAL-INT-SL/B An endoscope and accessories is a device used to provide access, illumination, and allow observ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2620-2024·2024-08-21

    Surgical light heads may detach due to weld defects

    DKK Dai-Ichi Shomei is recalling 293 Aurora surgical light heads because the frame welds can crack, potentially causing the light head to detach during use. No injuries have been reported.

    Product
    Aurora 3 Series, Aurora 7 lighthead; Models: AUT7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2574-2024·2024-08-21

    Merit Medical cardiac kits contain plastic syringes with quality defects

    Merit Medical convenience kits used in cardiac procedures contain plastic syringes with potential leaks and breakage. The defects were identified following an FDA Safety Alert issued March 19, 2024.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude SNAP (Introducer Catheter kit), REF: For the introduction of various types of pacing leads and catheters to the heart and coronary venous system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2577-2024·2024-08-21

    Merit Medical Catheter Kits Recalled for Syringe Leaks and Breakage Issues

    Merit Medical convenience kits containing defective plastic syringes are being recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects approximately 4,027 kits distributed nationwide.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG/Worley advanced CSG (Introducer Catheter kit), REF: FCL-083-02/A WOR-CSG-B1-09/A WOR-CSG-B2-09/A WOR-CSG-BL1-09/A WOR-CSG-E-90/A For the int
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2575-2024·2024-08-21

    Merit Medical Cardiac Catheter Kits Recalled for Syringe Leaks and Breakage

    Merit Medical's Prelude SNAP-H cardiac catheter kits are being recalled because their syringes may leak or break during use, potentially affecting cardiac procedures. No illnesses have been reported.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude SNAP-H (Introducer Catheter kit), REF: PLSH-1006/A PLSH-1007/A PLSH-1008/A PLSH-1009.5/A PLSH-2506/A PLSH-2507/A For the introduction of various t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2413-2024·2024-08-21

    Dental X-Ray Device Testing Defect May Affect Image Repeatability

    Palodex Group Oy recalls the Orthopantomograph OP300 dental x-ray system due to a testing software defect that may allow devices with poor image repeatability to be distributed.

    Product
    Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray device produces conventional 2D X-ray images and Xray projection images for the reconstruction of a 3D view. The device is operated and used by qualified healthcare professionals.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2586-2024·2024-08-21

    Heated Eye Mask Recalled Due to Detachable Wires and Burn Risk

    EYE COMFORT CARE LLC is recalling the UNclog Eye Mask due to safety clips that may allow wires to detach, potentially causing electrical shorts and burn injuries.

    Product
    Brand Name: UNclog Eye Mask Product Name: UNclog Eye Mask Model/Catalog Number: AG23JW24 Serial # ag22 Product Description: Heated eye mask Component: Heating unit, wire
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2566-2024·2024-08-21

    Merit Medical Pressure Monitoring Kits with Defective Syringes Recalled

    Merit Medical is recalling 69 convenience kits containing defective syringes that may leak or break, potentially risking patient safety during medical procedures. The kits were distributed nationwide.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K11 (Custom Pressure Monitoring Kit), REF: K11-00382C To support fluid administration into the body and physiological pressure monitoring. To support various v
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2580-2024·2024-08-21

    VITROS Folate Reagent Pack Recalled for Delayed Test Results

    Ortho-Clinical Diagnostics is recalling VITROS Folate Reagent Pack due to fibrinogen precipitation causing delayed test results. The recall affects 18,467 units distributed worldwide.

    Product
    VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2622-2024·2024-08-21

    Salivary Testosterone ELISA Quality Control Failure Invalidates Test Results

    DRG International is recalling Salivary Testosterone ELISA kits (Model SLV-3013) due to out-of-range quality controls that invalidate test runs and delay patient results. The recall affects 257 units distributed nationwide in six states.

    Product
    Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013 Product Description: An enzyme immunoassay for the quantitative in vitro diagnostic measurement of free active testosterone in saliva.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2545-2024·2024-08-21

    Discrete Chemistry Analyzer Recalled Due to Carousel Malfunction

    Beckman Coulter is recalling 59 units of its Access 2 Immunoassay System Analyzer due to misaligned index wheels causing carousel motion errors that disable the analyzer and cancel patient tests.

    Product
    Discrete photometric chemistry analyzer for clinical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24745·2024-08-15

    BJ's Warehouse Recalls Berkley Jensen Gazebos for Roof Panel Hazard

    BJ's Wholesale Club is recalling about 32,500 Berkley Jensen gazebos because roof panels can dislodge in high winds, causing injury. The company has reported 137 incidents, including one minor injury.

    Product
    Berkley Jensen Gazebos
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24340·2024-08-15

    Mamibaby and Cosy Nation Baby Loungers Recalled for Suffocation and Fall Hazards

    About 32,270 Mamibaby and Cosy Nation baby loungers sold on Amazon.com from June 2023 through June 2024 are being recalled because they violate federal infant sleep product regulations and pose suffocation, fall, and entrapment hazards to infants.

    Product
    Mamibaby and Cosy Nation Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24345·2024-08-15

    DeWALT Battery Walk-Behind Mowers Recalled for Laceration Hazard

    Stanley Black & Decker is recalling about 46,200 DeWALT Battery walk-behind mowers because water entering the handle support can cause the mower to fail to shut off or start without a key, posing a laceration risk.

    Product
    DeWALT Battery Push walk-behind mowers and DeWALT Battery Self-Propelled walk-behind mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24341·2024-08-15

    ALDI Recalls Ambiano Single Serve Coffee Makers for Burn Hazard

    ALDI is recalling about 28,000 Ambiano Single Serve Coffee Makers because the machines can expel hot water from the top, causing burns. ALDI has received 25 reports of this defect, including three burn injuries.

    Product
    Ambiano Single Serve Coffee Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24344·2024-08-15

    IKEA VARMFRONT Power Banks Recalled Due to Fire Hazard

    IKEA is recalling approximately 1,600 VARMFRONT Power Banks (models E2037 and E2038) because the devices can overheat and pose a fire hazard. No injuries have been reported in the United States.

    Product
    VARMFRONT Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24342·2024-08-15

    Trader Joe's Mango Tangerine Scented Candles Recalled for Fire Hazard

    Trader Joe's recalls 653,000 Mango Tangerine Scented Candles due to fire hazard—flame can spread from wick to wax. Fourteen incidents reported, including minor burns and property damage.

    Product
    Mango Tangerine Scented Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2442-2024·2024-08-14

    Medline Medical Procedure Kits Recalled Due to Defective Plastic Syringes

    Medline is recalling over 1.6 million medical procedure kits nationwide and internationally due to plastic syringe defects. The affected kits contain syringes with leaks, breakage, and quality issues that may pose risks to patient health.

    Product
    Medline procedure kits labeled as: 1) CONTINUOUS BLOCK, Pack Number DYNJRA0960C; 2) COMBINED SPINAL AND EPIDURAL, Pack Number DYNJRA1268C; 3) WAL- UNIVERSAL BLOCK TRAY, Pack Number DYNJRA1638C; 4) BASIC DIAGNOSTIC TRAY, Pack Number DYNJRA1928; 5) PREOP NERVE BLOCK TRAY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1671-2024·2024-08-14

    Palmer Candy and Meijer Popcorn Products Recalled for Salmonella

    Palmer & Company is recalling Palmer Candy Drizzled Caramel Corn and Meijer Drizzled Caramel Popcorn Snack Bowls due to potential Salmonella contamination. Products were distributed nationwide in the United States and Canada.

    Product
    1. Palmer Candy Drizzled Caramel Corn, Item 19271, Net Wt. 16/5oz tubs, UPC 77343 19271 2. Meijer Drizzled Caramel Popcorn Snack Bowl, Net Wt. 12oz, UPC 60236 18830, 8/12oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1667-2024·2024-08-14

    Palmer Candy Chow Down Mix Recalled Due to Potential Salmonella

    Palmer & Company is recalling Palmer Candy Chow Down Mix (Item 10731, 25 lbs, UPC 77232 10731) distributed nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Palmer Candy Chow Down Mix, Item 10731, Net Wt 25lbs, UPC 77232 10731
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1665-2024·2024-08-14

    Palmer Candy Munchy Medley products recalled due to potential salmonella contamination

    Palmer & Company is recalling multiple Munchy Medley candy and snack products nationwide due to potential salmonella contamination. Salmonella can cause serious illness in vulnerable populations.

    Product
    1. Palmer Candy Munchy Medley, Item 38004, Net Wt. 16/6oz bulk case, UPC 77232 38004 2. Palmer Candy Munch Medley, Item 10737, Net Wt. 15 lbs, UPC 77232 10737 3. Casey's Munchy Medley, Sweet & Salty Crunch Mix, Net Wt. 4.25 oz, UPC 98437 26083 6/case 4. Snackin' with the Crew! Mi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0626-2024·2024-08-14

    Dietary supplement tainted with undeclared pharmaceuticals recalled nationwide

    Umary Acido Hialuronico dietary supplement (850 mg caplets) was recalled nationwide by the FDA for containing undeclared Diclofenac and Omeprazole. The product was marketed without an approved drug application.

    Product
    Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0631-2024·2024-08-14

    Acetaminophen tablets incorrectly labeled with aspirin drug facts information

    Some bottles of Acetaminophen Extra Strength 500 mg tablets are labeled with the drug facts information for Aspirin 81 mg tablets. The affected lot is 4138197 (expiration 10/31/2025), distributed nationwide.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1672-2024·2024-08-14

    Palmer Patriotic Pretzels recalled for potential salmonella contamination

    Palmer & Company is recalling Palmer Patriotic Pretzels due to potential salmonella contamination. The affected products were distributed nationwide in the United States and Canada.

    Product
    1. Palmer Patriotic Pretzels, White & Chocolatey Fudge Covered Star Shaped Pretzels, Net Wt. 6oz, UPC 77232 37055, 16/6oz case 2. Palmer Patriotic Pretzels, White & Chocolatey Fudge Covered Star Shaped Pretzels, Net Wt 14 oz, UPC 7723237059, 12/14 oz case
    Category
    Food
    Distribution
    Distributed nationwide