The Recall Desk

State

Delaware product recalls

73,381 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.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20576–20600 of 76819

  • HighFDA (Devices)·Z-1498-2022·2022-08-10

    Atellica CH Iron_2 Diagnostic Device Produces False Microalbumin Results from Reagent Carryover

    Siemens Atellica CH Iron_2 in vitro diagnostic devices are being recalled because they produce falsely elevated microalbumin test results when a microalbumin test immediately follows an iron test. No illnesses have been reported.

    Product
    Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and (lithium heparin) plasma samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1303-2022·2022-08-10

    Matzim LA Extended-Release Tablets Recalled for Dissolution Specification Failure

    Matzim LA Extended-Release Tablets, 240 mg are being recalled due to failed dissolution specifications. Patients taking this medication should consult their doctor about their treatment.

    Product
    Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30-count bottles, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL USA 33314, USA, Distributed by: Actavis Pharma Inc., Parsippany, NJ 07054 USA; NDC 58544-692-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1537-2022·2022-08-10

    Vicks ZzzQuil Melatonin Syrup recalled for unapproved manufacturing process

    Procter & Gamble is recalling 90,522 cases of Vicks ZzzQuil Liquid Melatonin Syrup due to being an acidified/low-acid dietary supplement without an FDA-approved manufacturing process.

    Product
    Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bottle sold as single and twin pack
    Category
    Food
    Distribution
    45 states
  • HighFDA (Devices)·Z-1481-2022·2022-08-10

    Endoscopic Grasper Instruments Recalled Due to Weld Separation Risk

    Aesculap Implant Systems is recalling PRESTIGE ATRAUMATIC GRASPER surgical instruments because the weld connecting the handle to the shaft may separate during use.

    Product
    PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1302-2022·2022-08-10

    Prescription Drug Matzim LA Extended-Release Tablets Recalled for Failed Dissolution

    Teva Pharmaceuticals is recalling Matzim LA (Diltiazem Hydrochloride) 180 mg tablets because they failed to meet dissolution specifications. The recall affects approximately 8,022 bottles distributed nationwide in the United States and Puerto Rico.

    Product
    MATZIM LA — MATZIM LA (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V613000·2022-08-10

    Altec Recalls 2015-2022 Aerial Devices Due to Weld Crack Risk

    Altec Industries is recalling 2015-2022 DT65 and DT85 Aerial Devices because a weld crack could cause the auger bracket to detach, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1535-2022·2022-08-10

    Vicks Children's Botanicals Liquid Nighttime Recalled for Improper Processing

    The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Nighttime due to manufacturing without an approved acidification process. The product's preservation safety cannot be assured.

    Product
    Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle
    Category
    Drug
    Distribution
    45 states
  • HighFDA (Devices)·Z-1484-2022·2022-08-10

    E-100 Generator electrosurgical units recalled due to preventative maintenance oversight

    Intuitive Surgical is recalling 505 E-100 electrosurgical generators because required preventative maintenance was not performed on units distributed worldwide and in the US.

    Product
    The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and X systems. The E-100 is installed on the Vision Cart and is connected to the system. The functions of the E-100 are initiated by the foot pedals on the Surgeon…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1496-2022·2022-08-10

    Merlin 2 PCS MER3400 programmer software recalled by St. Jude Medical

    St. Jude Medical recalled Merlin 2 PCS MER3400 programmer software version 1.1.2 revision 1 or earlier in an FDA Class II recall. The recall affects 622 units distributed across the United States and internationally.

    Product
    Merlin 2 PCS MER37000 programmer Model MER3400 software
    Category
    Medical Device
    Distribution
    54 states
  • HighNHTSA·22V609000·2022-08-10

    2023 International Commercial Trucks and Buses: Engine Stall Defect

    Navistar is recalling 2023 International and IC Bus commercial vehicles because the engine control module may short-circuit, causing the engine to stall unexpectedly. This defect increases the risk of crashes.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS MV, TC, LT, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V616000·2022-08-10

    2021–2022 Pleasure Way Motorhomes Recalled for Mislabeled Electrical Circuit Board

    Pleasure Way is recalling 2021–2022 Rekon, Tofino, Ascent, Plateau, and Ontour motorhomes due to a mislabeled DCF4 circuit board. The board is labeled for 30 amps but has pins rated for only 20 amps, creating a fire risk.

    Product
    PLEASURE WAY — PLEASURE WAY PLATEAU, ASCENT, ONTOUR, TOFINO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1495-2022·2022-08-10

    Pacemaker Programmer Software May Display Overestimated Battery Longevity

    St. Jude Medical's Merlin PCS 3650 programmer software may display overestimated predicted battery longevity for certain pacemakers. This could affect clinical decision-making regarding device maintenance and replacement timing.

    Product
    Merlin PCS 3650 programmer Model 3330 software
    Category
    Medical Device
    Distribution
    54 states
  • HighFDA (Food)·F-1534-2022·2022-08-10

    Vicks Children's Botanicals Recalled for Unapproved Acidification Process

    The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Daytime dietary supplement due to use of an unapproved acidification process. The product was distributed to 42 states in approximately 34,526 cases.

    Product
    Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle
    Category
    Drug
    Distribution
    45 states
  • HighFDA (Devices)·Z-1499-2022·2022-08-10

    Craftmatic Model 1 Adjustable Bed Base Recalled for Separation Risk

    Craftmatic Industries is recalling the Model 1 Base for Dual Bed Configurations due to a potential for the bed bases to separate or slip apart. This defect could cause dual-configured beds to shift unexpectedly.

    Product
    Craftmatic Model 1 Base for Dual Bed Configurations
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1500-2022·2022-08-10

    Craftmatic Legacy Bed Base Recalled for Potential Separation Risk

    Craftmatic Industries recalls the Legacy Base for Dual Bed Configurations due to a potential for beds to separate or slip away from one another. The defect poses a risk of unintended bed movement.

    Product
    Legacy Base for Dual Bed Configurations
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V611000·2022-08-10

    Electric awning defect recalled in Thor Motor Coach motorhomes

    Thor Motor Coach is recalling 2022-2023 motorhomes whose electric retractable awning may drop due to a failing welded seam. This increases the risk of injury.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FOUR WINDS, QUANTUM, CHATEAU, GENEVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1533-2022·2022-08-10

    Vicks Children's Botanicals Liquid Supplement Recalled for Improper Processing

    The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Combo Pack because the acidified/low acid dietary supplement was manufactured without an FDA-approved process.

    Product
    Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles
    Category
    Drug
    Distribution
    45 states
  • HighFDA (Devices)·Z-1502-2022·2022-08-10

    UroLift System recalled for potential implant deployment failure

    Neotract Inc is recalling 18,722 UroLift Systems due to potential improper implant deployment during use. Patients should contact their healthcare provider.

    Product
    UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
    Category
    Medical Device
    Distribution
    45 states
  • HighFDA (Devices)·Z-1442-2022·2022-08-10

    NanoSight NS300 Medical Device Recalled for Laser Safety Noncompliance

    Malvern Panalytical is recalling 507 NanoSight NS300 units due to noncompliance with Class 1 laser safety requirements. The device may not meet established safety standards for laser-based instruments.

    Product
    NanoSight NS300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V615000·2022-08-10

    Lexus Recalls RC F Vehicles for Missing Tire Weight Label

    Lexus is recalling 2020-2022 RC F vehicles because the tire information label lacks the vehicle's weight capacity, which may increase crash risk.

    Product
    LEXUS — LEXUS RC F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V610000·2022-08-10

    2023 IC BUS CESB School Buses Engine Control Module Stall Risk

    Navistar is recalling certain 2023 IC CE school buses because the engine control module may experience an internal electrical short-circuit, causing the engine to stall unexpectedly. An unexpected engine stall increases the risk of a crash.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1501-2022·2022-08-10

    Turbett Surgical Container TS1500: Unapproved Rework Processes

    Turbett Surgical, Inc. is recalling the Turbett Surgical Container TS1500 because the affected units were subject to unapproved rework processes. Seven units were distributed to healthcare facilities in Colorado, Florida, North Carolina, and Pennsylvania.

    Product
    Turbett Surgical Container, TS1500
    Category
    Medical Device
    Distribution
    Distributed nationwide