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.

Which agencies issued them

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.

21251–21275 of 76826

HighFDA (Food)·F-1378-2022·2022-06-22
Potato Salad Recalled Nationwide for Metal Contamination Risk
Morski Brands recalled 832 units of Dawn's Smoked Gouda & Bacon Potato Salad due to possible metal fragments. Consumers with products bearing best-before dates 5-13-22, 6-21-22, 6-24-22, or 6-27-22 should not consume them.
Product
Dawn's Smoked Gouda & Bacon Potato Salad, #10079, Net Wt 8 lb (3.63 kg) Keep Refrigerated. UPC 10032345130019. Mfg By Morski Brands, Inc., Portage, WI 53901
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1144-2022·2022-06-22
Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Assurance Failure
Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension due to lack of assurance of sterility. The recall affects approximately 57,997 prefilled syringes distributed nationwide.
Product
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 16714-999-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1130-2022·2022-06-22
Homeopathic Drug Diphtherinum Recalled for Manufacturing Practice Deviations
Washington Homeopathic Products is recalling Diphtherinum homeopathic remedy (potencies 14C, 30C, 200C) distributed nationwide due to manufacturing practice deviations (cGMP violations). Affected lots: 20332, 20333.
Product
Diphtherinum, Potency: 14C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1127-2022·2022-06-22
Homeopathic Drug Recall: Candida Albicans Remedy for Manufacturing Quality Issues
Washington Homeopathic Products is recalling Candida Albicans homeopathic remedy due to manufacturing quality control violations. The voluntary recall affects 1,047 bottles distributed nationwide.
Product
Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C, 19C, 24C, 25C, 26C, 30C, 200C, 14X, 15X, 16X, 20X, 288X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1128-2022·2022-06-22
Candida Parapsilosis homeopathic remedy recalled for manufacturing practice deviations
Washington Homeopathic Products is recalling Candida Parapsilosis homeopathic remedies distributed nationwide due to manufacturing practice deviations. The recall affects 134 bottles under lot numbers 22315 and 26502.
Product
Candida Parapsilosis, Potency: 14X, 15X, 16X, 20X, 28X, 30X, 9C, 10C, 13C, 15C, 25C, 30C, 13X, 27X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1158-2022·2022-06-22
Artri Ajo King Tablets Recalled for Unapproved Drug Claims
Walmart is recalling all lots of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets nationwide. The product was marketed without FDA approval based on unapproved labeling claims.
Product
Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1140-2022·2022-06-22
Drug recall: Tuberculinum Bovinum due to manufacturing practice deviations
Washington Homeopathic Products is recalling Tuberculinum Bovinum homeopathic remedy due to current good manufacturing practice deviations. No illnesses have been reported.
Product
Tuberculinum Bovinum, Potency: 12C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1141-2022·2022-06-22
Homeopathic Drug Recall: Vaccinotoxinum Products Due to Manufacturing Violations
Washington Homeopathic Products is recalling Vaccinotoxinum homeopathic remedies (lot numbers 2512K and 20280) distributed nationwide due to cGMP manufacturing deviations. The voluntary recall was initiated by the firm in May 2022.
Product
Vaccinotoxinum, Potency: 32X, 11C, 30C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1129-2022·2022-06-22
Homeopathic Colibacillinum Drug Recall Due to Manufacturing Deviations
Washington Homeopathic Products recalls Colibacillinum homeopathic drug products due to manufacturing practice deviations. The recall involves 206 bottles distributed nationwide; the manufacturer voluntarily initiated it in May 2022.
Product
Colibacillinum, Potency: 12C, 14C, 15C, 18C, 20C, 30C, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1133-2022·2022-06-22
Homeopathic Drug Morbillinum Recalled for Manufacturing Practice Deviations
Washington Homeopathic Products is recalling Morbillinum in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.
Product
Morbillinum, Potency:7C, 8C, 9C, 10C 12C, 13C, 15C, 20C, 21C, 30C, 200 C,Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1148-2022·2022-06-22
Premium Nature Hand Sanitizer Recalled for Subpotent Ethanol Content
AMS Packaging is recalling Premium Nature Instant Hand Sanitizer nationwide because FDA analysis found some bottles contain less ethanol than labeled.
Product
Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML plastic bottles; Premium Nature, South Plainfield, NJ. UPC 819192028668
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1159-2022·2022-06-22
Artri King Reforzado con Ortiga Omega 3 Tablets Recalled as Unapproved Drug
Walmart Inc is recalling Artri King Reforzado con Ortiga Omega 3 Tablets nationwide because the product was marketed as a drug without FDA approval. All lots are affected.
Product
Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1139-2022·2022-06-22
Homeopathic Tuberculinum Drug Recalled for Manufacturing Practice Deviations
Washington Homeopathic Products is recalling Tuberculinum homeopathic drug in multiple potencies due to manufacturing practice deviations. The voluntary recall affects product distributed nationwide.
Product
Tuberculinum, Potency: 1X, 12X, 24X, 30X, 1M, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1132-2022·2022-06-22
Medorrhinum homeopathic drug recalled for manufacturing process deviations
Washington Homeopathic Products recalled Medorrhinum liquid pellets nationwide due to deviations from manufacturing standards. The product was distributed in 49 glass amber bottles.
Product
Medorrhinum, Potency:12C, 30C, 200C, 1M, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1136-2022·2022-06-22
Pyrogenium Homeopathic Remedy Recalled for Manufacturing Process Violations
Washington Homeopathic Products is recalling Pyrogenium homeopathic remedies in multiple potencies due to current Good Manufacturing Practice (cGMP) deviations. The firm initiated this voluntary recall affecting 6,782 bottles distributed nationwide.
Product
Pyrogenium, Potency: 15X, 16X, 17X, 19X, 21X, 22X, 25X, 30X, 1M, 200C, 30C, OTC, Liquid Pellets, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1137-2022·2022-06-22
Streptococcinum Homeopathic Drug Recalled Due to Manufacturing Deviations
Washington Homeopathic Products is voluntarily recalling Streptococcinum homeopathic drug in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.
Product
Streptococcinum, Potency: 8C, 9C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1134-2022·2022-06-22
Homeopathic Drug Pertussinum Recalled Due to Manufacturing Deviations
Washington Homeopathic Products is recalling Pertussinum in multiple potencies nationwide due to manufacturing practice deviations. Affected lot numbers are 18829, 20142, and 25410.
Product
Pertussinum, Potency: 19C, 30C, 200C, 1M, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1131-2022·2022-06-22
Homeopathic drug Influenzinum recalled for manufacturing process deviations
Washington Homeopathic Products is recalling Influenzinum in multiple potencies due to manufacturing process deviations. The recall affects approximately 6,400 units distributed nationwide.
Product
Influenzinum, Potency: 9X, 10X, 12X, 15X, 25X, 30X, 200C, 12C, 30C 1M, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1138-2022·2022-06-22
Syphilinum homeopathic drug recalled for manufacturing practice deviations
Washington Homeopathic Products is recalling Syphilinum homeopathic products in multiple potencies due to current good manufacturing practice deviations. The affected products were distributed nationwide.
Product
Syphilinum, Potency: 9C, 30C, 200C, 10X, 12X, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1125-2022·2022-06-22
Homeopathic Drug Anthracinum Recalled Over Manufacturing Compliance Deviations
Washington Homeopathic Products is recalling Anthracinum liquid pellets due to manufacturing process deviations. The voluntary recall affects 219 bottles distributed nationwide.
Product
Anthracinum, Potency: 6C, 7C, 8C, 9C, 12C, 14C, 30C, 200C, 11X, 14X, 30X Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22E052000·2022-06-21
Proterra Recalls High Voltage Junction Box DC Links for Electrical Defect
Proterra is recalling 185 High Voltage Junction Box DC Links because a battery cable may not be properly connected, risking power loss, ground short circuits, or fire.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM: CABLES recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V440000·2022-06-21
Fabform Recalls 2018-2022 Trailers Due to Utility Gate Stop Defect
Fabform is recalling 2018-2022 FLR-D, FLRR-D, and DBX trailers because a rubber stop may break, allowing the utility gate to detach and increase crash risk.
Product
FABFORM — FABFORM DBX, FLR-D, FLRR-D
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V439000·2022-06-20
Thomas Built Buses Recalling 2019-2023 Models for Engine Shutdown Risk
Daimler Trucks North America is recalling 258 Thomas Built Buses and FCCC Saf-T-Liner models due to a software defect that may cause unexpected engine shutdowns, increasing crash risk.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES, FCCC SAF-T-LINER C2, S2G
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V438000·2022-06-20
School Bus Engine Control Module Defect May Cause Unexpected Shutdown
Daimler Trucks recalls certain Thomas Built school buses (2020-2023) due to an engine control module defect that can cause unexpected engine shutdown while driving, increasing crash risk.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E051000·2022-06-20
BorgWarner Recalls EGR Valves Due to Risk of Loss of Drive Power
BorgWarner is recalling specific EGR valves where a loose washer may cause the valve to stick open, resulting in an unexpected loss of drive power.
Product
ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:EMISSION CONTROL:GAS RECIRCULATION VALVE (EGR VALVE) recall
Category
Vehicle
Distribution
Distributed nationwide