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.

26851–26875 of 77004

  • HighFDA (Devices)·Z-1293-2021·2021-03-31

    Mizuho Operating Table Hand Control Units Recalled for Sliding Risk

    Mizuho OSI is recalling 26 operating table hand control units because they may cause the tabletop to slide in the opposite direction, potentially delaying surgical procedures.

    Product
    Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage: intended to support a patient during surgical operations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2021·2021-03-31

    In2Bones Shannon Percutaneous Burr Recalled for Potential Breakage During Use

    In2Bones is recalling 60 units of Shannon Percutaneous Burrs due to manufacturing non-conformity that may cause the burr to break during surgery.

    Product
    In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot mini-invasive and percutaneous surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1290-2021·2021-03-31

    Corin Trinity Hip Prosthesis Heads Recalled for Incorrect Size Labeling

    Corin Ltd is recalling 23 units of Trinity Biolox Delta Ceramic Heads due to incorrect size labeling on packaging and patient stickers.

    Product
    Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1304-2021·2021-03-31

    Cardinal Health Recalls Femoral Angiography Drapes Due to Sticking Defect

    Cardinal Health is recalling non-sterile femoral angiography drapes because a manufacturing defect causes them to stick, preventing proper application.

    Product
    Femoral Angiography Drape Bulk Non-Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1300-2021·2021-03-31

    Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance

    Cardinal Health is recalling In-View Clear Leggings Sterile because a manufacturing variance causes the plastic film to stick, potentially preventing proper application.

    Product
    In-View Clear Leggings Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1279-2021·2021-03-31

    Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability

    Baxter Healthcare is recalling 1,650 Prismaflex Control Units used for renal replacement therapy because tubing performance variability may cause alarms during or after system self-tests.

    Product
    Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1291-2021·2021-03-31

    Corin Trinity Acetabular System Recalled for Incorrect Size Labeling

    Corin Ltd is recalling 23 units of the Trinity Acetabular System because the size indicated on the packaging and patient stickers is incorrect.

    Product
    Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1302-2021·2021-03-31

    Cardinal Health Recalls In-View Clear Leggings Due to Sticking Defect

    Cardinal Health is recalling In-View Clear Leggings because a manufacturing variance causes the plastic film to stick, preventing proper application.

    Product
    In-View Clear Leggings Bulk Non-Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1295-2021·2021-03-31

    Ortho-Clinical Diagnostics Recalls VITROS TIBC Calibrator Kits Due to Performance Shift

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 4 and Fe Slides because TIBC results may be approximately 80 ug/dL lower than expected.

    Product
    VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC only). Used to calibrate VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and VITROS 5600/XT 7600 Integrated Systems Product Code: 1204668 Impacted Products: A. VITROS Chemistry Products TIBC Kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1277-2021·2021-03-31

    Baxter Recalls Prismaflex Control Units Due to Tubing Performance Variability

    Baxter Healthcare is recalling Prismaflex Control Units because tubing variability may cause alarms during self-tests. The units are used for Continuous Renal Replacement Therapy.

    Product
    Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1288-2021·2021-03-31

    Siemens Recalls 29 Interventional Fluoroscopic X-Ray Systems for Shutdowns

    Siemens is recalling 29 interventional fluoroscopic X-ray systems because the power supply may cause the computer to shut down unexpectedly.

    Product
    Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V220000·2021-03-30

    Dennis Eagle Elite and Proview Recalled for Incorrect ABS Warning Light

    Dennis Eagle is recalling 2017-2021 Elite and Proview vehicles because the ABS warning light may illuminate incorrectly when brake pads wear out, potentially causing driver confusion.

    Product
    DENNIS EAGLE — DENNIS EAGLE PROVIEW, ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E024000·2021-03-30

    Cummins Recalls Electric Drivetrain Parts Due to High Voltage Shock Risk

    Cummins is recalling Electric Drivetrain part number PD7000 because it cannot detect isolation faults, posing a high voltage shock risk to service personnel.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:SHOCK PROTECTION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V223000·2021-03-30

    2020-2021 Lincoln Aviator vehicles recalled for backup camera display failure

    Ford is recalling 2020-2021 Lincoln Aviator vehicles because the backup camera display may not show video feed, affecting rear visibility. Free software updates are available from Ford dealers.

    Product
    LINCOLN — LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V221000·2021-03-30

    2021 Alfa Romeo Stelvio Side Curtain Air Bag May Fail to Deploy

    2021 Alfa Romeo Stelvio vehicles may have improperly crimped clamps in the side curtain air bag assembly, which can fail to deploy in a crash, increasing injury risk. Chrysler will replace the assemblies at no cost.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V222000·2021-03-30

    Pierce Recalls 2016-2018 Trucks Due to Excessively Bright Rear LED Lights

    Pierce Manufacturing is recalling 2016-2018 Enforcer, Freightliner, and Saber trucks because rear LED lights may be too bright, potentially blinding other drivers.

    Product
    PIERCE — PIERCE FREIGHTLINER, ENFORCER, SABER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E023000·2021-03-30

    Nado LED Headlight Bulb Recall for Excessive Glare and Brightness

    Nado Stuff is recalling MICTUNING LED headlight bulbs that create excessive glare, increasing crash risk. Owners will receive a full refund.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E022000·2021-03-30

    BEAMTECH LED Headlight Bulbs Recalled for Excessive Glare and Brightness

    Guangzhou Lengzhilu Trading Co., Ltd. is recalling specific BEAMTECH LED headlight bulbs because they create excessive glare, failing federal safety standards.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V218000·2021-03-29

    Winnebago Recalls 2020 Minnie RVs Due to Incorrect Tire Labeling

    Winnebago is recalling 2020 Minnie vehicles because the Tire and Loading Information label lists the wrong tire size, which could lead to improper tire installation and increased crash risk.

    Product
    WINNEBAGO — WINNEBAGO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V219000·2021-03-29

    2021 Forest River Berkshire Class A Motorhomes: Brake Light Reflection Defect

    Forest River is recalling certain 2021 Berkshire Class A motorhomes due to brake lights that may not adequately reflect light. The defect affects visibility and compliance with Federal Motor Vehicle Safety Standards.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V217000·2021-03-26

    Mercedes-Benz Recalls AMG Models Due to Starter Cable Fire Risk

    Mercedes-Benz is recalling 493 AMG E63S and GT63 models because an incorrectly installed starter cable may chafe wires, causing a short circuit, vehicle stall, or fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, AMG GT63, AMG GT63S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V216000·2021-03-26

    2020 Mercedes-Benz E-Class passenger seat limiter safety recall

    Mercedes-Benz is recalling certain 2020-2021 E-Class and AMG models due to a passenger seat limiter defect that may allow the seat to position too close to the frontal airbag, increasing injury risk during airbag deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, AMG E53, AMG E63S, E63 AMG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21732·2021-03-25

    Polaris Recalls Ranger and Utility Vehicles Due to Fire Hazard

    Polaris is recalling approximately 41,500 Ranger, ProXD, Gravely, and Bobcat off-road vehicles because a drive belt can break, damage the fuel line, and cause a fire.

    Product
    Model Year 2020-2021 RANGER 1000 and RANGER CREW 1000, Model Year 2020 ProXD 2000G and 4000G, Model Year 2020-2021 Ariens/Gravely JSV3200, JSV3400, and JSV6400, Model Year 2020 Bobcat UV34 4x4 GAS and UV34 XL GAS, and Model Year 2021 Bobcat UV34 4x4 GAS
    Category
    Consumer Product
    Distribution
    Distributed nationwide