The Recall Desk

State

Delaware product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26801–26825 of 77004

  • HighFDA (Drugs)·D-0318-2021·2021-04-07

    Ferring Recalls ZOMA-Jet 10 Demonstration Kits Due to Defective Delivery System

    Ferring Pharmaceuticals is recalling 1,569 ZOMA-Jet 10 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.

    Product
    ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial, ZOMA-Jet 10 Demonstration Kit contains -ZOMA-Jet 10 device - 7 Needle-Free Head A's - 1 Carrying Case - 1 User Manual; Manufactured for: Ferring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1315-2021·2021-04-07

    DePuy Orthopaedics Recalls Mobile Bearing Total Knee Systems Due to Packaging Damage

    DePuy Orthopaedics is recalling specific lots of the LCS COMPLETE P.F.C. SIGMA RP Mobile Bearing Total Knee System because of potential damaged packaging.

    Product
    The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee System - Product Usage: consists of three components intended to replace the femoral, tibial, and patellar articular surfaces of the knee joint.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1329-2021·2021-04-07

    Oscor SafeSheath ULTRALITE 10F Recalled for Potential Open Sterile Seal

    Oscor, Inc. is recalling 500 units of the AngioDynamics SafeSheath ULTRALITE 10F due to a potential open seal on the sterile product.

    Product
    AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various types of pacing leads and catheters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1327-2021·2021-04-07

    Stryker Harmonic ACE +7 Shears Recalled for Lack of Regulatory Clearance

    Stryker is recalling 102 units of Harmonic ACE +7 Shears because they were distributed without receiving regulatory clearance.

    Product
    Stryker Sustainability Solutions REF HARH36 Ethicon Endo-Surgery, Inc. Harmonic ACE +7, Shears with Advanced Hemostasis 5mm Diameter x 36cm - Product Usage: indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired. The instruments can be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1312-2021·2021-04-07

    LumiraDx Coronavirus Antigen Test Strips Recalled for False Positives

    LumiraDx is recalling 2,186 coronavirus antigen test strips because two lots failed quality control testing and produced false positives.

    Product
    Coronavirus antigen detection test system - Product Usage: intended for the qualitative detection of the nucleocapsid protein antigen to SARS-CoV-2 directly from nasal swab samples collected from individuals suspected of COVID-19 by their healthcare provider within the first…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1316-2021·2021-04-07

    DePuy ATTUNE Rotating Platform Total Knee System Recalled for Damaged Packaging

    DePuy Orthopaedics is recalling 355 units of the ATTUNE Rotating Platform Total Knee System due to potential damaged packaging. The affected tibial bases are used in cemented total knee arthroplasty.

    Product
    The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Usage: consists of multiple components intended to replace the femoral, tibial, and patellar articular surfaces of the knee joint.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1314-2021·2021-04-07

    DePuy ATTUNE Knee Implant Recall for Damaged Packaging

    DePuy Orthopaedics is recalling ATTUNE and MBT tibial base components used in knee replacements due to potential damaged packaging.

    Product
    ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components designed to replace the natural articular surface of the knee joint. The femoral component is a metal implant without a porous coating. The tibial component may…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1310-2021·2021-04-07

    Arthrex Recalls Cannulated Drill Bits Due to Incorrect Color Indicator

    Arthrex, Inc. is recalling 9 units of 5.0 mm cannulated drill bits because the color indicator on the shaft is the incorrect color.

    Product
    Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V241000·2021-04-06

    Mercedes-Benz and Freightliner Sprinter Recalled for Steering Hose Defect

    Daimler Vans USA is recalling 2019-2020 Sprinter vans because hydraulic power steering hoses may detach, causing fluid leaks and loss of steering assist.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER (VS30), SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V242000·2021-04-06

    Arcimoto Electric Motorcycles Recalled for Inverter Firmware Defect

    Arcimoto is recalling 2019-2021 FUV, 2020-2021 Deliverator and Roadster, and 2021 Rapid Responder motorcycles. A firmware defect in the inverter may cause the vehicle's battery to shutdown without warning, increasing the risk of a crash.

    Product
    ARCIMOTO — ARCIMOTO ROADSTER, DELIVERATOR, FUV, RAPID RESPONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V236000·2021-04-05

    2021 Forest River Flagstaff and Rockwood Fifth Wheels Pin Box Defect

    Forest River is recalling certain 2021 Flagstaff and Rockwood fifth wheels due to pin box defects. The pin box may be under-rated for the vehicle's gross weight rating, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·21V237000·2021-04-05

    Mercedes-Benz Sprinter VIN Mismatch Recall

    Daimler Vans USA is recalling one 2019 Mercedes-Benz Sprinter because its VIN numbers do not match, potentially preventing owners from receiving safety recall notices.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V234000·2021-04-04

    2021 INFINITI Q50 and Q60 Engine Control Module Software Defect

    INFINITI is recalling 2021 Q50 and Q60 vehicles for an Engine Control Module software defect that may cause engine stall and increase crash risk. Dealers will reprogram the ECM software free of charge.

    Product
    INFINITI — INFINITI Q60, Q50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·pha-04022021-01·2021-04-02

    USDA Issues Public Health Alert for Raw Ground Chorizo Sausage

    USDA FSIS issued a public health alert for raw ground chorizo sausage due to possible contamination with hard crystalline material. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert for Raw Ground Chorizo Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·011-2021·2021-04-01

    Rong Shing Trading Recalls Ineligible Chinese Beef Hot Pot Base

    Rong Shing Trading Inc. is recalling approximately 3,365 pounds of Chinese-style hot pot base containing beef tallow imported from China, a country ineligible to export beef to the U.S.

    Product
    Rong Shing Trading Inc. Recalls Ineligible Beef Products Imported from China
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V229000·2021-04-01

    Mercedes-Benz Recalls Vehicles for Steering Shaft Bearing Separation Risk

    Mercedes-Benz is recalling specific 2017-2018 models because a steering shaft defect could cause loss of control. Dealers will inspect and replace the shaft free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250, CLA250, AMG CLA45, AMG GLA45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21735·2021-04-01

    BATTOP Foldable Infant Bath Seats Recalled for Drowning Hazard

    BATTOP is recalling about 5,000 foldable infant bath seats sold on Amazon.com because they can tip over, posing a drowning risk to babies.

    Product
    Foldable Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21734·2021-04-01

    doTERRA Recalls Essential Oils Due to Non-Child-Resistant Packaging

    doTERRA is recalling 1.3 million bottles of Deep Blue, PastTense, and Deep Blue Touch essential oils because the packaging is not child-resistant, posing a poisoning risk.

    Product
    doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V233000·2021-04-01

    Mack heavy trucks recalled for electronic stability control software malfunction

    Mack trucks (2018-2022) with electronic stability control may drift out of their lane at certain speeds, increasing crash risk. Dealers will reprogram the control units free of charge.

    Product
    MACK — MACK PINNACLE (CHU), GRANITE (GR), GRANITE (GU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V230000·2021-04-01

    2021 Mercedes-Benz Vehicles Recalled for Faulty Seat Switch

    2021 Mercedes-Benz vehicles are being recalled due to a faulty seat position switch that may prevent airbags and seatbelt force limiters from activating during a crash. MBUSA will replace the switches free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450, C 300, E 350, AMG GT63S
    Category
    Vehicle
    Distribution
    Distributed nationwide