The Recall Desk

State

Delaware product recalls

73,486 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.

What the numbers show

Total
3,438
Critical
477
Severe
1,110
Most recent
2026-10-14

Of the 3,438 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,110 (32%) are Severe.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24026–24050 of 76924

  • SevereFDA (Food)·F-0190-2022·2021-11-24

    HelloFresh Meal Kits Recalled for Salmonella Contamination

    HelloFresh is recalling certain meal kits containing onions from ProSource that are associated with a Salmonella Oranienburg outbreak. The affected kits have Product Codes 2-5-8-9-16-19-21-22-23-24-25 from Production Week 29 (starting July 14, 2021) and were distributed nationwide.

    Product
    HelloFresh Meal Kit Product Code 2-5-8-9-16-19-21-22-23-24-25 from Production Week 29 (production week start date: 07/14/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0201-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella Contamination

    HELLOFRESH US is recalling specific EveryPlate meal kits containing onions from ProSource linked to a Salmonella Oranienburg outbreak. The affected products were produced in week 31, 2021.

    Product
    EveryPlate Meal Kit Product Codes 82-83-84-90-91-92-94-96-97-100 from Production Week 31 (production week start date: 07/28/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0206-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella-Contaminated Onions

    EveryPlate meal kits distributed nationwide are being recalled because they contain onions purchased from ProSource that are associated with a Salmonella Oranienburg outbreak.

    Product
    EveryPlate Meal Kit Product Codes 82-83-89-93-94-96-98 from Production Week 36 (production week start date: 09/01/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0204-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella Contamination Risk

    EveryPlate meal kits with specific product codes from production week 34 (starting 08/18/2021) are being recalled nationwide because onion ingredients from ProSource are associated with a Salmonella Oranienburg outbreak.

    Product
    EveryPlate Meal Kit Product Codes 82-84-85-87-88-90-92-97-98 from Production Week 34 (production week start date: 08/18/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0233-2022·2021-11-24

    Arrow-Trerotola Percutaneous Thrombolytic Device inner lumen detachment and embolization risk

    Arrow-Trerotola PTD catheters are being recalled because the inner lumen can detach from the device basket, causing embolization that requires additional intervention. 1,167 units are affected.

    Product
    Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-W The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0200-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella Contamination

    HelloFresh US is recalling specific EveryPlate meal kits containing onions contaminated with Salmonella Oranienburg. The affected products are from production week starting July 21, 2021, with product codes 84, 88, 89, 90, 91, 92, 94, 98, 99, and 100.

    Product
    EveryPlate Meal Kit Product Codes 84-88-89-90-91-92-94-98-99-100 from Production Week 30 (production week start date: 07/21/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0236-2022·2021-11-24

    Syphilis Test Calibrator Recalled for False-Positive Reactivity Issues

    Bio-Rad BioPlex 2200 Syphilis calibrator set (791 units, Lot 52953) is recalled due to elevated test reactivity that does not confirm with treponemal tests and potential early shelf-life failure causing measurement bias.

    Product
    BIO-RAD BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL The BioPlex 2200 Syphilis Total & RPR Calibrator Set is intended for the calibration of the BioPlex 2200 Syphilis Total & RPR Reagent Pack.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0237-2022·2021-11-24

    LOTRIMIN AF Jock Itch Powder Spray Recalled for Benzene Contamination

    Bayer Healthcare is recalling LOTRIMIN AF Jock Itch Powder Spray (Miconazole nitrate 2%, 4.6 OZ cans) distributed nationwide due to manufacturing facility cGMP deviations where other lots were found to be contaminated with benzene.

    Product
    LOTRIMIN AF (Miconazole nitrate 2%) Jock Itch Powder Spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-4140-2. UPC 3 11017 41031 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0226-2022·2021-11-24

    Sensis Diagnostic System UI Freeze Risk Without Regular System Reboots

    Siemens' Sensis diagnostic systems may experience partial UI freezing and fail to update vital signs display if not rebooted at least every 7 days per manufacturer instructions.

    Product
    Sensis/ Sensis Vibe systems with software VD1X as follows: (1)Sensis Model 10764561 (2) Sensis Vibe Hemo Model 11007641 (3)Sensis Vibe Combo Model 11007642 Intended Use: A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0258-2022·2021-11-24

    LEEP PRECISION Integrated System may fail to coagulate during surgery

    CooperSurgical is recalling 75 units of the LEEP PRECISION Integrated System due to a defect where the hand switch may not activate the coagulation function, potentially causing prolonged surgery and bleeding complications.

    Product
    LEEP PRECISION Integrated System, 220V CooperSurgical part numbers: LP-10-220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0229-2022·2021-11-24

    Beaver Xstar Crescent Knife surgical blades recalled for specification mismatch

    Beaver Visitec is recalling CustomEyes surgical kits where Crescent Knives contain bevel-up blades instead of the specified bevel-down blades. The specification error could affect surgical precision during cataract procedures.

    Product
    bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component REF# 58000572 REF#: 373809
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0262-2022·2021-11-24

    Electrosurgical Generator Coagulation Function May Fail During Surgery

    CooperSurgical recalled 700 Quantum 2000 Electrosurgical Generators due to a hand switch coagulation function defect that may fail to operate during surgery, potentially requiring medical intervention to control intraoperative bleeding.

    Product
    Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0235-2022·2021-11-24

    Syphilis Test Reagent Pack Recalled Due to False Positive Results

    Bio-Rad is recalling 11,610 units of BioPlex 2200 syphilis test reagent packs because they can produce false positive results that don't confirm with follow-up tests, due to elevated reactivity and shelf-life issues.

    Product
    BIO-RAD BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack The BioPlex Syphilis Total & RPR kit is a multiplex flow immunoassay intended for the qualitative detection of total (IgG/IgM) antibodies to Treponema pallidum and the qualitative detection and/or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V925000·2021-11-24

    RAM Pickup Trucks Side Air Bag Deployment Defect Recall

    Chrysler is recalling certain 2021-2022 RAM 2500 and 3500 pickup trucks and 2021 RAM 1500 Classic models. The side air bag curtain assemblies may deploy improperly due to incorrect gas pressure, increasing injury risk in a crash.

    Product
    RAM — RAM 2500, 3500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0230-2022·2021-11-24

    Surgical Crescent Knife Recalled for Incorrect Blade Orientation Labeling

    Beaver Visitec International is recalling bvi CustomEyes Kits containing Crescent Knives due to incorrect labeling. Products labeled as 55-degree bevel-down blades actually contain bevel-up blades.

    Product
    bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component-non-sterile sample for evaluation purposes REF# BVI 58000587
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0259-2022·2021-11-24

    LEEP PRECISION Generator 120V Hand Switch Coagulation Function Failure

    CooperSurgical is recalling 244 LEEP PRECISION Generator 120V units because the hand switch's coagulation function may fail to operate properly, potentially requiring medical intervention to control bleeding during surgical procedures.

    Product
    LEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V924000·2021-11-24

    Harley-Davidson Recalls 2021 Pan America Motorcycles for Seat Base Defect

    Harley-Davidson is recalling 2,689 2021 Pan America RA1250 motorcycles because the seat base may not be fastened properly, posing an injury risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON PAN AMERICA (RA1250)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0245-2022·2021-11-24

    Tinactin Tolnaftate Powder Spray Recalled for Potential Benzene Contamination

    Bayer Healthcare is recalling Tinactin (Tolnaftate 1%) Powder Spray due to potential benzene contamination from cGMP deviations at the manufacturing facility. The recall affects approximately 2.8 million cans distributed nationwide and internationally.

    Product
    Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) can, Labeled as (a) Product of Ireland 86940418, (b)Product of Finland 20006106, (c) Product of Ireland with Instant redeemable coupon ( IRC); Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 3…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0240-2022·2021-11-24

    Lotrimin Daily Prevention Deo Spray Recalled for Benzene Contamination Risk

    Bayer Healthcare Pharmaceuticals is recalling Lotrimin Daily Prevention Deo (Tolnaftate) spray due to potential benzene contamination from manufacturing facility cGMP deviations. The product was distributed nationwide and internationally.

    Product
    LOTRIMIN DAILY PREVENTION DEO — LOTRIMIN DAILY PREVENTION DEO (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0261-2022·2021-11-24

    Quantum 2000 Electrosurgical Generator Hand Switch Coagulation Failure

    CooperSurgical Quantum 2000 Electrosurgical Generators may fail to coagulate tissue when using the hand switch during surgery, potentially extending procedures and requiring medical intervention to control intraoperative bleeding. The Class II recall affects 193 units.

    Product
    Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0243-2022·2021-11-24

    Tinactin Tolnaftate Spray Recalled for Potential Benzene Contamination

    Bayer Healthcare is recalling Tinactin (Tolnaftate 1%) liquid spray due to potential benzene contamination. The product was manufactured at a facility where other lots were found to be contaminated with benzene.

    Product
    TINACTIN — TINACTIN (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0250-2022·2021-11-24

    REGARD Basic Cataract Tray Recalled for Out-of-Specification Component

    ROi CPS LLC is recalling 126 REGARD Basic Cataract trays because a Povidone-Iodine swabstick component is out of specifications. Affected trays were distributed in Florida, Louisiana, and Missouri.

    Product
    REGARD Basic Cataract tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0255-2022·2021-11-24

    REGARD Ultrasound Trays Recalled for Out-of-Specification Swabstick Component

    ROi CPS LLC has recalled REGARD Ultrasound Trays because they contain out-of-specification Povidone-Iodine swabstick components. The 240 affected trays were distributed in Florida, Louisiana, and Missouri.

    Product
    REGARD Ultrasound Tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0251-2022·2021-11-24

    REGARD Core Biopsy Tray Recalled for Out-of-Specification Component

    ROi CPS LLC recalled 1,200 REGARD Core Biopsy Trays distributed nationwide because a Povidone-Iodine swabstick component supplied by PDI, Inc. was manufactured out of specifications.

    Product
    REGARD Core Biopsy Tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0266-2022·2021-11-24

    Cobas u 601 urinalysis analyzer recalled for false negative nitrite results

    Roche Diagnostics is recalling the Cobas u 601 urinalysis test system due to potential false negative nitrite results when endogenous creatinine levels exceed 15,000 mg/L. The device may fail to detect nitrite in urine samples with elevated creatinine.

    Product
    Cobas u 601 urinalysis test system, Catalog number 06334601001 The cobas U 601 urinalysis test system is comprised of the cobas u 601 urine analyzer and the cobas u pack. The cobas u 601 urine analyzer when used with the cobas u pack is a fully automated urinalysis system…
    Category
    Medical Device
    Distribution
    Distributed nationwide