State

Delaware product recalls

73,219 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: 939
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 939 (27%) are Severe.

Which agencies issued them

These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16826–16850 of 76657

HighCPSC·23752·2023-05-04
L.O.L. Surprise! Metal Doll Pins Recalled for Excessive Lead Paint
Culture Fly is recalling approximately 6,600 L.O.L. Surprise! Trick or Treat subscription boxes sold with metal doll pins because the paint on the pins contains lead levels that exceed the federal lead paint ban, posing a lead poisoning hazard to young children.
Product
L.O.L. Surprise! Trick or Treat subscription boxes sold with Metal Doll Pins
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23754·2023-05-04
Children's White Robes Recalled for Flammability Standards Violation
The Company Store is recalling about 930 children's white robes sold online from September 2021 through November 2022 because they fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk.
Product
Children's white robes
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V326000·2023-05-04
Altec Recalls 2017-2022 Digger Derricks Due to Missing Hardware
Altec is recalling 2017-2022 Digger Derricks because missing hardware may allow the auger extension bar to detach, increasing injury risk.
Product
ALTEC — ALTEC DIGGER DERRICK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V320000·2023-05-04
Gas Leak Risk in Horse Trailers and Sprinter Vans with Faulty Cooktops
Outback Customs is recalling certain 2020-2023 horse trailers and 2021-2022 Sprinter Vans equipped with SDS2 cooktops. Aluminum burner tubes may fracture and leak gas, increasing fire risk.
Product
PLATINUM — PLATINUM, CIMARRON, OUTBACK CUSTOM HORSE TRAILER, SPRINTER, DODGE RAM RCA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V317000·2023-05-04
Ferrara Recalls 2022 Fire Trucks Due to Winch Remote Water Intrusion
Ferrara Fire Apparatus is recalling 2022 Ultra and Inferno fire trucks because water in the winch remote can cause corrosion and unintentional operation.
Product
FERRARA — FERRARA ULTRA, INFERNO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V319000·2023-05-04
PJ Trailers Coupler May Loosen and Separate, Posing Crash Risk
PJ Trailers is recalling certain 2022-2024 trailers with Demco EZ Latch Gooseneck Couplers because the mounting bolts may loosen, causing the coupler to separate and creating a crash risk.
Product
PJ TRAILERS — PJ TRAILERS LS, LD, LX, LY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V324000·2023-05-04
2022-2023 Land Rover Range Rover Second-Row Armrest Latch Failure Recall
Jaguar Land Rover is recalling 2022-2023 Range Rover vehicles because the second-row armrest latch may fail, allowing unsecured objects to strike occupants during a crash. Dealers will replace the locking arm free of charge.
Product
LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23C004000·2023-05-04
Baby Trend Recalls Hybrid 3-in-1 Booster Seats Due to Latch Webbing Fraying
Baby Trend is recalling approximately 2,600 Hybrid 3-in-1 Combination Booster Seats because the latch assembly webbing may fray, potentially failing to restrain a child in a crash.
Product
CHILD SEAT:LATCH STRAP recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V325000·2023-05-04
Entegra and Jayco Class B RVs Recalled: Fuel Hose Clamp Defect
Jayco, Inc. is recalling certain 2021-2024 Class B recreational vehicles. A fuel hose clamp may be inadequate, potentially causing gasoline leaks and increasing fire risk.
Product
ENTEGRA — ENTEGRA, JAYCO ETHOS, SWIFT, SOLSTICE, EXPANSE
Category
Vehicle
Distribution
Distributed nationwide
ModerateCPSC·23753·2023-05-04
Sahara Folding Food Dehydrators Recalled for Fire Hazard
Berkshire Innovations is recalling about 990 Sahara Folding Food Dehydrators because the heater fan can fail and cause the unit to overheat, posing a fire hazard. No injuries or property damage have been reported.
Product
Sahara Folding Food Dehydrators
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23196·2023-05-04
Severe Weather Doorglass Inserts Recalled Due to Wind-Borne Debris Risk
ODL Inc. is recalling Severe Weather Doorglass Inserts sold at Home Depot and Lowe's because the adhesive bond can separate during hurricanes, creating a risk of injury and property damage from windborne debris.
Product
Severe Weather Doorglass Inserts
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0802-2023·2023-05-03
Savor Imports IQF Raspberries recalled for potential Hepatitis A contamination
Savor Imports IQF Whole Raspberries (Lot 20220210) are recalled nationwide due to potential Hepatitis A contamination. Consumers should not eat the product and should return or discard it.
Product
Savor Imports IQF Whole Raspberries; Net Wt 2-5lb; MFG# 341798; UPC: 10684476003771
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·23V314000·2023-05-03
Bentley Recalls Flying Spur Vehicles Due to Screen Bracket Defect
Bentley is recalling 2021-2023 Flying Spur vehicles because an incorrectly installed rear entertainment screen bracket could become a projectile in a crash, increasing injury risk.
Product
BENTLEY — BENTLEY FLYING SPUR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2023·2023-05-03
Draeger Infinity M300 Patient Monitor Software Displays Inaccurate ECG Readings
Draeger Infinity M300/M300+ patient monitoring systems may display or print ECG waveforms with inaccurate QRS amplitudes due to software peaks being dropped on narrow waveforms.
Product
Draeger Infinity M300 and M300+, for use with the ICS to monitor ECG and pulse oximetry on ambulatory and non-ambulatory adult and pediatric patients using wireless communication over the Infinity patient monitoring network,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1466-2023·2023-05-03
Stryker ORTHOLOC 3Di Fusion Plate Contains Incorrect Laser Markings
Wright Medical Technology recalls Stryker ORTHOLOC 3Di Fusion Plate MTP Right devices due to incorrect dorsiflexion descriptions laser marked on the parts. 41 units distributed nationwide.
Product
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1425-2023·2023-05-03
Surgical forceps may fail to open during endoscopic procedures
Richard Wolf surgical forceps may fail to open when the endoscope shaft is bent. Affected units distributed worldwide; users should check lot numbers and discontinue use if affected.
Product
FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1436-2023·2023-05-03
Sterile surgical C-section kit light handle covers recalled for separation risk
ROi CPS LLC recalls sterile surgical C-section kits due to light handle covers that may separate and fall during use. The recall affects 1,312 kits distributed in Florida and Missouri.
Product
Sterile surgical convenience kit: regard Item Number 800706005, LD0091E - OH C-Section Pack.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1423-2023·2023-05-03
Biopsy forceps may fail to open when endoscope is bent
Biopsy forceps may become unable to open when the endoscope shaft is bent approximately 90 degrees. Additional bending of the forceps shaft can prevent opening entirely.
Product
FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0554-2023·2023-05-03
Tadalafil Tablets Recalled Due to Manufacturing Practice Violations
Northwind Pharmaceuticals is recalling 23 bottles of Tadalafil 5 mg tablets nationwide due to manufacturing process deviations. The FDA classified this as a Class II recall.
Product
TADALAFIL — TADALAFIL (TADALAFIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0569-2023·2023-05-03
Fyremadel Ganirelix Acetate Injection Recalled for Glass Contamination
Sun Pharmaceutical is recalling 24,194 prefilled syringes of Fyremadel (ganirelix acetate) injection due to glass contamination found in a unit from lot HAD1190A. The recall affects units distributed nationwide with expiration 02/2024.
Product
FYREMADEL — FYREMADEL (GANIRELIX ACETATE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V315000·2023-05-03
Capacity Recalls 2022 TJ Series Trucks Due to Missing Seat Clip
Capacity of Texas is recalling 2022 TJ 5000, 6500, and 9000 trucks because a missing safety clip on the passenger jump seat could allow it to fall, increasing injury risk.
Product
CAPACITY — CAPACITY TJ 9000, TJ 6500, TJ 5000
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1467-2023·2023-05-03
Stryker ORTHOLOC 3Di Fusion Plate Recalled for Incorrect Marked Descriptions
Wright Medical Technology is recalling Stryker ORTHOLOC 3Di Fusion Plate MTP Right surgical implants due to incorrect dorsiflexion descriptions laser marked on 50 units distributed nationwide.
Product
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1463-2023·2023-05-03
VersaOne Reusable Positioning Cannula Recalled for Internal Metal Burr
Covidien LP is recalling 145 units of the VersaOne Reusable Positioning Cannula due to a manufacturing defect that may create a metal burr inside the device at the weld joint.
Product
VersaOne Reusable Positioning Cannula 8 mm Standard, Model Number RC8STS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1432-2023·2023-05-03
Sterile Surgical Kits Recalled Due to Light Handle Cover Separation Risk
ROi CPS LLC is recalling 662 sterile surgical convenience kits because light handle covers may separate from the light handle and fall off during use. The kits were distributed in Florida and Missouri.
Product
Sterile surgical convenience kits: 1. regard Item Number: 880353009, GS00797I - Laparotomy Pk; 2. regard Item Number: 880429002, GS01036B - Universal Custom ; 3. regard Item Number: 800725004, GS00930D - OH Base Robot Pack ; 4. regard Item Number: 800725005, GS00930E…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1461-2023·2023-05-03
GEM NEUROTUBE Nerve Repair Mesh Recalled for Brittleness and Potential Crumbling
Baxter Healthcare's GEM NEUROTUBE absorbable mesh tube, used for peripheral nerve repair, is recalled because the product is brittle and may crumble when handled or removed from packaging. The recall affects 169 units distributed worldwide.
Product
GEM NEUROTUBE, Absorbable Woven Polyglycolic Acid Mesh Tube, Product Codes: a) 5311-01240-010, b) 5311-01240-012; for peripheral nerve repair
Category
Medical Device
Distribution
Distributed nationwide