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.

21126–21150 of 76826

  • HighFDA (Devices)·Z-1310-2022·2022-07-06

    FDA Recalls TEG 5000 Fibrinogen Reagent Kits Due to Outdated Reference Ranges

    Haemonetics Corporation is recalling TEG 5000 Functional Fibrinogen Reagent kits because the reference ranges in the instructions have shifted. Clinicians using these outdated ranges could misdiagnose patients or fail to provide necessary treatment.

    Product
    TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1308-2022·2022-07-06

    Surgical Light Paint Particles May Fall Into Operating Field

    Paint particles may detach from VOLISTA StandOP Surgical Lights and fall into the operating field during surgery, risking infection and organ irritation. Getinge Usa Sales Inc is recalling 337 affected units in the United States.

    Product
    VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP ARD568811961 VLT600DF AIM STP ARDVST229000A VST60SF AIM ARDVST229001A VST60DF AIM ARDVST229002A VST66SF AIM ARDVST229003A VST66DF AIM ARDVST229034A…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1384-2022·2022-07-06

    Wilton Rainbow Sprinkles Mix recalled for milk contamination

    Wilton Industries recalled 16,281 units of Wilton Rainbow Sprinkles Mix due to milk contamination. The affected lots are 21005Z and 21111Z.

    Product
    Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1305-2022·2022-07-06

    Laparoscopic irrigator recalled for inability to provide irrigation

    Davol, Inc. is recalling the HydroSurg Plus Laparoscopic Irrigator because the device cannot provide irrigation as intended. The recall affects 4,390 units in the US and 390 in Canada.

    Product
    HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Cojoined Suction and Irrigation Tubing, Catalog Number 0026870
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1299-2022·2022-07-06

    Radiation therapy software shows misleading dose display in RayStation 11B

    RayStation 11B radiation therapy planning software has two display issues affecting Linear Energy Transfer values. These errors could lead to incorrect dose calculations if not identified during clinical review.

    Product
    RayStation 11B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1170-2022·2022-07-06

    Calcipotriene Scalp Solution Recalled Due to Defective Delivery System

    Akorn, Inc. is recalling Calcipotriene Topical Solution 0.005% (Scalp Solution) nationwide due to a defective delivery system that could prevent the product from dispensing properly.

    Product
    Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, N.Y. 11701. NDC: 50383-732-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1301-2022·2022-07-06

    IVUS Catheter Recall: Missing Contraindications in Instructions

    Volcano Corp is recalling Visions PV. 035 Digital IVUS Catheters because instructions for use do not include contraindications information. Healthcare providers should contact the manufacturer for complete safety documentation before use.

    Product
    Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1302-2022·2022-07-06

    Digital IVUS Catheter Recalled for Missing Contraindication Information

    Volcano Corp is recalling 7,520 units of the Volcano Visions PV. 035 Digital IVUS Catheter due to missing contraindication information in the instructions for use. The IFU lacks details about situations where the device should not be used.

    Product
    Volcano Visions PV. 035 Digital IVUS Catheter REF 81234, PN: 300007367341 , Rx Only, Sterile EO, CE 2797
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1288-2022·2022-07-06

    FDA recalls MAC laryngoscope sets due to packaging error

    Baxter Healthcare Corporation is recalling MAC laryngoscope devices due to a packaging error. The recall affects 99 units distributed worldwide.

    Product
    #1 MAC F/O LARYNGOSCOPE; F/O Laryngoscope Set-MAC; F/O Laryngoscope Set-MAC W/LED
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1303-2022·2022-07-06

    Fresenius Optiflux 200NRe Dialyzers Recalled Due to Temperature Exposure

    Fresenius Medical Care is recalling 19 cases of Optiflux 200NRe dialyzers distributed in Pennsylvania after exposure to cold temperatures outside safe storage ranges. Affected lot number is 22AU04017.

    Product
    Optiflux 200NRe Dialyzer Finished Assy., Model no. 0500320E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V466000·2022-07-01

    Mercedes-Benz Recalls 2020 GLS Models for Front Air Bag Wiring Defect

    Mercedes-Benz is recalling 2020 GLS 450 and GLS 580 vehicles because the front air bag wiring harness may be routed incorrectly, potentially preventing proper air bag deployment in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 580 4MATIC, GLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V472000·2022-07-01

    Silver Eagle Recalls 2021 VAST-20W Trailer Converter Dollies

    Silver Eagle is recalling 2021 VAST-20W trailer converter dollies because a ballast hanger may fail and fall onto the roadway, creating a road hazard.

    Product
    SILVER EAGLE — SILVER EAGLE VAST-20W
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V471000·2022-07-01

    Audi Recalls A4 and A8 Models for Airbag Inflator Defect

    Audi is recalling 1997-1998 A4 and 1998 A8 vehicles because the driver's airbag inflator may explode or underinflate, posing a risk of injury.

    Product
    AUDI — AUDI A4, A8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V475000·2022-07-01

    Autocar Recalls 2022-2023 Trucks Due to Steering Gear Fracture Risk

    Autocar is recalling 2022-2023 Legend, Xpeditor, and Xspotter trucks because incorrectly assembled steering gears may fracture, causing loss of steering control.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, XSPOTTER, LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V467000·2022-07-01

    Mercedes-Benz Recalls 2022 EQS Models for Bumper Tow Ring Defect

    Mercedes-Benz is recalling 2022 EQS 450, EQS 580, and AMG EQS 53 vehicles because the bumper tow ring assembly may detach, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 580, EQS 450, AMG EQS 53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V474000·2022-07-01

    2022 Oliver Legacy Elite II Travel Trailer Bearing Washer Recall

    The 2022 Oliver Travel Trailers Legacy Elite II may have a cracked bearing washer in the hub assembly that could cause the hub to separate from the axle, risking loss of vehicle control. Owners should contact Oliver at 1-866-205-2621 for a free replacement.

    Product
    OLIVER TRAVEL TRAILERS — OLIVER TRAVEL TRAILERS LEGACY ELITE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V473000·2022-07-01

    2022 Subaru Outback Engine Wiring Harness Damage Causes Stall Risk

    The engine wiring harness may be damaged in 2022 Subaru Outback vehicles, causing a loose connection to the engine control unit. This could cause engine stalls and increase crash risk.

    Product
    SUBARU — SUBARU OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22177·2022-06-30

    Children's Pajamas Recalled for Flammability Standards Violation

    Kids Tales-branded children's pajamas fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 9,100 units sold online at Amazon from November 2021 through April 2022 are affected.

    Product
    Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V468000·2022-06-30

    Freightliner recalls 2022 Cascadia trucks for parking brake failure

    Daimler Trucks is recalling certain 2022 Freightliner Cascadia trucks because the electronic parking brake may fail to engage when turned off, risking vehicle rollaway. Owners should contact dealers for free repair.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22175·2022-06-30

    RIO-Branded Swinging Hammock Chairs Recalled Due to Collapse Injury Hazard

    ShelterLogic Group is recalling approximately 786,000 RIO-branded swinging hammock chairs because improper pin insertion during assembly can cause the chair's legs to collapse, injuring users. The company has received 24 reports of injuries including bruises, lacerations, concussions, and back strain.

    Product
    RIO-branded Swinging Hammock Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22754·2022-06-30

    Mohnark Lidocaine 4% Topical Anesthetic Cream Recalled for Non-Child-Resistant Packaging

    Mohnark Pharmaceuticals is recalling Lidocaine 4% Topical Anesthetic Cream because the packaging does not meet child-resistant requirements, creating a poisoning risk if young children ingest the product. About 9,000 units sold online were affected.

    Product
    Lidocaine 4% Topical Anesthetic Cream
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22176·2022-06-30

    Laars Residential Gas-Fired Boilers Recalled for Carbon Monoxide Risk

    Laars Heating Systems is recalling about 545 residential gas-fired boilers because a malfunctioning blocked vent temperature switch can release carbon monoxide into homes. No injuries have been reported.

    Product
    Residential atmospheric gas-fired boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V465000·2022-06-30

    GM Recalls 2018-2020 Buick Regal for Brake Software Error

    General Motors is recalling 2018-2020 Buick Regal vehicles because a software error may cause loss of power brake assist, increasing stopping distance.

    Product
    BUICK — BUICK REGAL
    Category
    Vehicle
    Distribution
    Distributed nationwide