The Recall Desk

State

Delaware product recalls

73,388 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
2026-09-23

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.

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21051–21075 of 76826

  • ModerateFDA (Devices)·Z-1324-2022·2022-07-13

    Intervertebral fusion device recalled for outer carton labeling discrepancy

    DePuy Spine's EIT CIF intervertebral fusion cage (46 units, Part No. CUI8070S) is recalled due to a labeling discrepancy where the outer carton label does not match the labels on the product packaging and patient materials.

    Product
    EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD) Part Number: CUI8070S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1323-2022·2022-07-13

    EIT CIF Cage Intervertebral Fusion Device Carton Labeling Mismatch Recall

    DePuy Spine is recalling 61 units of the EIT CIF cage spinal fusion device due to a labeling mismatch. The outer carton label does not match the labels on the blister packages and patient information labels.

    Product
    EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD). Part Number: CUI8060L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1178-2022·2022-07-13

    Enalapril Maleate Tablets Recalled Due to Manufacturing Practice Deviations

    Golden State Medical Supply Inc. is recalling Enalapril Maleate Tablets due to manufacturing practice deviations. The voluntary recall involves 9,058 units distributed nationwide.

    Product
    ENALAPRIL MALEATE — ENALAPRIL MALEATE (ENALAPRIL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1182-2022·2022-07-13

    Doxycycline oral suspension recalled for insanitary manufacturing conditions

    Wedgewood Village Pharmacy LLC is recalling Doxycycline oral suspension (10 mg/ml, 60 ml bottles) nationwide due to insanitary conditions and lack of processing controls discovered during FDA inspection.

    Product
    Doxycycline (as Calcium) (equivalent to 50mg/5mL), 10 mg/ml, 60 ml suspension bottles, Peppermint, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Dr, Ste 200, Swedesboro, NJ 08085
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1181-2022·2022-07-13

    Bethanechol Chloride suspension recalled due to insanitary manufacturing conditions

    Wedgewood Village Pharmacy is recalling Bethanechol Chloride 1mg/ml suspension (lot 000-03715131) due to insanitary conditions and lack of processing controls observed during an FDA inspection.

    Product
    Bethanechol Chloride 1mg/ml, 80 ml Suspension bottles Banana/Strawberry, Qty:1, Wedgewood Village Pharmacy LLC, 405 Heron Dr. Ste 200, Swedesboro, NJ 08085
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1342-2022·2022-07-13

    Siemens X-ray System Fan Wear May Cause Equipment Malfunction

    Siemens is recalling 88 Artis Icono X-ray systems in the U.S. due to increased fan wear that could lead to electrical failure and malfunction of the imaging system during operation.

    Product
    Artis Icono, Interventional Fluoroscopic X-Ray System, Model No. 11327600
    Category
    Medical Device
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-1177-2022·2022-07-13

    Prescription drug Enalapril Maleate recalled for manufacturing deviations

    Golden State Medical Supply Inc. is recalling Enalapril Maleate 2.5 mg tablets due to Current Good Manufacturing Practice (CGMP) deviations. Approximately 1,471 bottles were distributed nationwide.

    Product
    ENALAPRIL MALEATE — ENALAPRIL MALEATE (ENALAPRIL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1176-2022·2022-07-13

    Testosterone Cypionate Injectable Drug Recalled for Manufacturing Deviations

    Sun Pharmaceutical is recalling 27 vials of Testosterone Cypionate Injection (200 mg/mL) due to manufacturing deviations caused by abnormal machinery appearance. The recall affects multiple lot numbers distributed nationwide.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1173-2022·2022-07-13

    Mometasone Furoate Topical Solution Recalled Due to Defective Containers

    Glenmark Pharmaceuticals is recalling Mometasone Furoate Topical Solution USP 0.1% due to defective containers. Approximately 98,307 packs were distributed nationwide.

    Product
    MOMETASONE FUROATE — MOMETASONE FUROATE (MOMETASONE FUROATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V499000·2022-07-12

    Vermeer Recalls 2022 BC1800XL Trailers Due to Hitch Bolt Defect

    Vermeer is recalling 2022 BC1800XL trailers because improper hitch bolts may fail, causing the trailer to separate and increasing crash risk.

    Product
    VERMEER — VERMEER BC1800XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-07122022-01·2022-07-12

    Trader Joe's Caesar Salad with Chicken Alert for Undeclared Egg Allergen

    USDA issued a public health alert for Trader Joe's Caesar Salad with Chicken because the dressing packets contain undeclared egg. No illnesses have been reported.

    Product
    F&S Produce West LLC — FSIS Issues Public Health Alert for Ready-to-Eat Caesar Salad with Chicken Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V495000·2022-07-11

    Prevost Recalls 2021 X3-45 Commuter Buses Due to Missing Seat Bolt

    Prevost is recalling 30 units of the 2021 X3-45 commuter bus because a bolt securing the rear bench seat was not installed, creating a crash injury risk.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V494000·2022-07-11

    Mercedes-Benz Recalls 2020 GLC 350 E Vehicles for Transmission Wiring Defect

    Mercedes-Benz is recalling 1,168 2020 GLC 350 E vehicles because a transmission wiring harness may chafe against the drive shaft, causing loss of drive power and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V491000·2022-07-11

    Mercedes-Benz Recalls 2021 Sprinter 2500 for Electrical Surge Risk

    Daimler Vans USA is recalling 2021 Mercedes-Benz Sprinter 2500 vehicles because an incorrectly connected generator wiring harness may cause an electrical surge, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V496000·2022-07-11

    Prevost Recalls 2021-2023 X3-45 Commuter Buses Due to Seat Defect

    Prevost is recalling 2021-2023 X3-45 commuter buses because a seat retention pin could fail, causing the backrest to collapse and increasing injury risk in a crash.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V493000·2022-07-11

    Mercedes-Benz Recalls Vehicles Due to Rearview Camera Display Failure

    Mercedes-Benz is recalling 8,530 vehicles because a software error may prevent the rearview camera from displaying images, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH EQS 580, S 580, AMG EQS 53, S 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V498000·2022-07-11

    BIG TEX 16GN trailers recalled for faulty spare tire mount

    Big Tex Trailer Manufacturing is recalling 2003-2022 16GN trailers with defective spare tire mounts that may detach, creating a road hazard.

    Product
    BIG TEX — BIG TEX 16GN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V490000·2022-07-11

    Eveland Scamp Travel Trailers Recalled for Gas Leak Risk

    Eveland is recalling 2022 Scamp travel trailers because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    EVELAND — EVELAND SCAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V485000·2022-07-08

    2020-2021 Subaru Outback and Legacy vehicles recalled for transmission control defect

    Subaru is recalling certain 2020-2021 Outback and Legacy vehicles for a transmission control unit programming error that may cause the drive chain to slip, resulting in loss of drive power and increased crash risk.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V487000·2022-07-08

    Coachmen Freelander Motorhomes Recalled for Propane Valve Defect

    Forest River is recalling certain Coachmen Freelander and other motorhomes due to improperly connected LPG service valves that can cause propane leaks and fire risk. Dealers will inspect and replace valves at no cost.

    Product
    DYNAMAX — DYNAMAX, COACHMEN ISATA, FREELANDER, PURSUIT, SPORTSCOACH
    Category
    Vehicle
    Distribution
    Distributed nationwide