State

Delaware product recalls

72,933 recalls have nationwide distribution and so reach Delaware. 3,435 additional recalls listed Delaware specifically in their distribution scope.

What the numbers show

Total: 3,435
Critical: 477
Severe: 937
Most recent: 2026-09-09

Of the 3,435 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 937 (27%) are Severe.

Which agencies issued them

These figures cover only the 3,435 recalls whose distribution notice names Delaware specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2776–2800 of 76368

SevereFDA (Devices)·Z-1547-2026·2026-03-18
TRUE METRIX AIR manuals recalled as Class I over E-5 guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX AIR blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/REA4002-01, CVS TRUE METRIX AIR Kit/REA4007-01, GNP TRUE METRIX AIR Kit/REA4011-
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1546-2026·2026-03-18
TRUE METRIX PRO manuals recalled as Class I over E-5 guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX PRO blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/RE4H01P-43, PROCURE TRUE METRIX PRO Meter Only/RE4212P-00, Henry Schein TRUE MET
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0400-2026·2026-03-18
Icosapent ethyl capsules recalled after active ingredient oxidized inside capsule
Zydus Pharmaceuticals is recalling eight lots of Icosapent Ethyl Capsules 1 gram after red dots and melted capsules were found, caused by oxidation of the active ingredient.
Product
ICOSAPENT ETHYL — ICOSAPENT ETHYL (ICOSAPENT ETHYL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2026·2026-03-18
Link Endo-Model SL connection component recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/07 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1557-2026·2026-03-18
Vital Sync remote monitoring may not receive bedside monitor alarms
Covidien is recalling the HealthCast Vital Sync Remote Patient Monitoring System after complaints that alarms from the primary patient bedside monitor were not transmitted to or received by the remote system.
Product
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 10884521844940 Vital Sync 3.4.1 / 10884521847569 (OUS Only) Vital Sync 3.4.2 /
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1541-2026·2026-03-18
GEM Premier 5000 part 00055445004 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055445004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055445004.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1512-2026·2026-03-18
Link Endo-Model plateau 15-0027/15 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/15;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1543-2026·2026-03-18
GEM Premier 5000 parts 00055445010 and 00055445011 may eject cartridges
Instrumentation Laboratory is recalling GEM Premier 5000 parts 00055445010 and 00055445011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up.
Product
GEM Premier 5000; Part No. 00055445010 & 00055445011.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1523-2026·2026-03-18
Link Endo-Model plateau 15-0027/16 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/16 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/16;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1537-2026·2026-03-18
GEM Premier 5000 part 00055430004 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430004 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055430004.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1536-2026·2026-03-18
GEM Premier 5000 part 00055415011 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No: 00055415011.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1538-2026·2026-03-18
GEM Premier 5000 part 00055430008 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055430008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1533-2026·2026-03-18
GEM Premier 5000 part 00055415005 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415005 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415005.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1530-2026·2026-03-18
GEM Premier 5000 PAK part 00055407510 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407510 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055407510.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2026·2026-03-18
Medline Medcrest surgical gowns may delaminate prematurely after recommended laundering
Medline is recalling Medcrest surgical gowns because the fabric may delaminate prematurely when the included laundering instructions are followed.
Product
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL DBD-GOWN,SURG,XALT,L4,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2026·2026-03-18
Link Endo-Model plateau 15-2835/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2835/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-2835/12;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1521-2026·2026-03-18
Link Endo-Model plateau 15-0027/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1555-2026·2026-03-18
Artelon FlexBand Plus implants failed bacterial endotoxin testing
International Life Sciences is recalling Artelon FlexBand Plus, refs 41054 and 41057, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FlexBand Plus Ref: 41054 & 41057
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2026·2026-03-18
Link Endo-Model plateau 15-8030/12 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8030/12 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8030/12;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1519-2026·2026-03-18
Link Endo-Model plateau 15-8521/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1544-2026·2026-03-18
Infant and child defibrillator electrodes recalled over pediatric electrode delamination
Physio-Control is recalling Infant/Child Reduced Energy Defibrillator Electrodes, catalogue numbers 11101-000016 and 11101-000017, due to pediatric defibrillator electrode delamination.
Product
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11101-000017 UDI-DI code: 00721902682483 Infant/Child Reduced Energy Defibrillation Electrodes are pre gelled, self-adhesive, the
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2026·2026-03-18
Link Endo-Model plateau 15-2836/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2836/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-2836/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1540-2026·2026-03-18
GEM Premier 5000 part 00055430011 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055430011.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1534-2026·2026-03-18
GEM Premier 5000 part 00055415008 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415008.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V162000·2026-03-18
Lexus NX, RX, and TX rearview camera software malfunction recall
Toyota is recalling certain 2022–2026 Lexus NX, RX, and TX vehicles because the rearview camera image may fail to display when the vehicle is in reverse, reducing rear visibility and increasing crash risk.
Product
LEXUS — LEXUS NX, RX, TX
Category
Vehicle
Distribution
Distributed nationwide