Delaware recalls
1,914 federal recalls affecting Delaware in the last 12 months: 40 sold in Delaware plus 1,874 sold nationwide. From the CPSC, FDA, USDA and NHTSA.
Recent recalls
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Big Way Hot Pot Miso Paste recalled for undeclared milkSold nationwide. Big Way Hot Pot's Hot Pot Miso Paste (1kg packages) contains milk that is not declared on the label. The product was distributed to two affiliated restaurants. This poses a risk to people with milk allergies or lactose intolerance.
ModerateFDAAug 12, 2026Big Way Hot Pot
Zydus mirabegron extended-release tablets recalled for N-nitroso impuritySold nationwide. Zydus Pharmaceuticals is recalling one lot of Mirabegron Extended-Release 25 mg tablets due to higher-than-acceptable levels of N-Nitroso Mirabegron impurity. This impurity can potentially increase long-term health risks with continued use. No injuries have been reported.
ModerateFDAAug 12, 2026Zydus
- Sunny Pharmtech cyclophosphamide recalled for stainless steel particulate
Sold nationwide. Cyclophosphamide for Injection, USP (1 gram/vial) manufactured by Sunny Pharmtech Inc. for Long Grove Pharmaceuticals may contain stainless steel particulate matter. The contamination was identified in two specific lots before distribution was completed.
SeriousFDAAug 12, 2026Sunny Pharmtech2 products
- Aurobindo Dicyclomine capsules recalled for empty capsules
Sold nationwide. Aurobindo Pharma USA is recalling Dicyclomine Hydrochloride Capsules 10mg (Batch DMC125018A, expiration 07/2027) because some bottles contain empty capsules instead of the medication. The issue affects approximately 6,408 bottles distributed nationwide.
ModerateFDAAug 12, 2026Aurobindo Pharma
Vitasia Asian Style Wok Spice Mix recalled for Salmonella riskLidl US is recalling Vitasia Asian Style Wok Spice Mix (1.58 oz, Lot #155846, Best By JUN 2028) because routine testing found potential Salmonella contamination. The affected product was sold at Lidl stores in Delaware, DC, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia between July 24 and August 10, 2026. No illnesses have been reported.
SeriousFDAAug 11, 2026Lidl
Schwarzkopf Professional Osis Grip mousse recalled for potential explosion riskSold nationwide. Schwarzkopf Professional Osis Grip extra strong mousse in 6.76 fl. oz aluminum cans may leak under pressure due to a packaging defect, creating a risk of explosion. The affected product was sold to salons and retailers across the U.S. Henkel learned of the issue through one customer complaint and two salon reports, with one instance of hand bruising reported.
SeriousFDAAug 11, 2026Schwarzkopf Professional
Fresenius Kabi Tyenne injection recalled for glass particlesSold nationwide. Fresenius Kabi recalled one lot of Tyenne (tocilizumab-aazg) Injection 400 mg/20 mL vials after discovering the product contains glass particles. The affected lot was distributed nationwide to hospitals, clinics, and distributors.
SeriousFDAAug 10, 2026Fresenius Kabi
Meat and poultry products with FDA-recalled jalapeños under Salmonella alertSold nationwide. The USDA found that multiple meat and poultry products contain jalapeños contaminated with Salmonella bacteria. The contaminated jalapeños came from an FDA-regulated supplier. No illnesses have been reported yet, but the products are being recalled out of caution.
SeriousUSDAAug 8, 2026
- Midamar, Bea's Best, Kirsch deli meats recalled for possible Listeria
Sold nationwide. City Foods, Inc. is recalling ready-to-eat pastrami and corned beef products because they may be contaminated with Listeria, a bacterium that can cause serious illness. The contamination was discovered during routine testing.
SeriousUSDAAug 8, 2026Midamar
Food to Live green powder recalled for Salmonella riskSold nationwide. Lexunder Inc., doing business as Food To Live, is recalling multiple green powder products (wheatgrass, spirulina, algae mix, and SuperGrass powders) because they may be contaminated with Salmonella. The company learned of the potential contamination after the FDA tested a retail sample. No illnesses have been reported so far.
SeriousFDAAug 7, 2026Lexunder
Apeks XL4 scuba regulators recalled for drowning riskSold nationwide. Certain Apeks second stage scuba regulators (models XL4, XL4+, and XL4 Ocea) can restrict air flow to divers at depths beyond 147 feet, creating a serious breathing hazard underwater. The affected regulators were sold between April 2025 and June 2026 and can be identified by serial numbers laser-etched on the side of the equipment.
SeriousCPSCAug 6, 2026Head
Laziza 3-in-1 dressers recalled for tip-over and entrapment riskSold nationwide. Fitueyes' Laziza wooden dressers can tip over if not anchored to the wall, creating a serious hazard for children. The dressers don't meet federal safety standards for furniture stability. About 150 units were sold online through Wayfair from March 2024 to April 2026.
SeriousCPSCAug 6, 2026Fitueyes
Courant Spliced Kalimba climbing ropes recalled for fall riskSold nationwide. The spliced ends on certain Courant Spliced Kalimba climbing ropes can fail unexpectedly during use. These ropes are designed for tree climbing and arborist work. The manufacturer has received three reports of splice failures, though no injuries have been reported yet.
SeriousCPSCAug 6, 2026Courant
KC Imports laser pointer keychains recalled for battery ingestion riskSold nationwide. KC Imports Mini Laser Pointer Keychains contain button cell batteries that children can access and swallow. Ingesting these batteries can cause serious internal injuries, chemical burns, and death. The product also lacks required safety warnings.
SeriousCPSCAug 6, 2026KC Imports and Exports
Syera LED finger lights recalled for battery ingestion riskSold nationwide. Syera LED finger light toys sold on Temu contain button cell batteries that children can easily access and swallow. Ingesting these batteries can cause serious internal chemical burns and other life-threatening injuries.
SeriousCPSCAug 6, 2026Syera
Little Rawr pull string teething toys recalled for choking riskSold nationwide. The silicone pull strings on this teething toy are longer and thicker than safety standards allow. The strings can reach the back of a child's throat and become lodged, causing choking or difficulty breathing. One child has already been injured this way.
SeriousCPSCAug 6, 2026Okabesini
EEMB battery chargers recalled for coin battery ingestion riskSold nationwide. EEMB lithium coin battery chargers contain easily accessible batteries that are not in child-resistant packaging and lack required safety warnings. If swallowed, these small batteries can cause serious internal burns and death.
SeriousCPSCAug 6, 2026A2batt
Voomf mattresses recalled for entrapment and fire risksSold nationwide. Voomf play yard and crib mattresses sold on Amazon may not fit properly in certain play yards, creating dangerous gaps where a baby could become trapped and suffocate. The full-sized crib mattresses also fail to meet flammability safety standards, posing a fire risk.
SeriousCPSCAug 6, 2026Voomf
Liuqibax bed rails recalled for entrapment and asphyxiation riskSold nationwide. Liuqibax adult portable bed rails (Model BR-11) do not meet safety standards and can trap users between the rail and mattress, creating a risk of serious injury or death by asphyxiation. The rails also lack required hazard warning labels. About 12,000 units were sold on Amazon between July 2024 and May 2026.
SeriousCPSCAug 6, 2026Luqiba
PIXLABBY magnetic fidget sliders recalled for magnet ingestion riskSold nationwide. These colorful silicone fidget sliders contain loose high-powered magnets that can be removed and swallowed. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injury including intestinal perforation, blockage, and blood poisoning. A child has already been hospitalized after ingesting magnets from one of these sliders.
SeriousCPSCAug 6, 2026PIXLABBY
Wnttmt baby walkers recalled for fall and entrapment riskSold nationwide. These infant walkers can pass through standard doorways and fail to stop at stairs, creating a fall hazard. They also have leg openings that allow children to slip down until their head becomes trapped. The walkers violate mandatory safety standards for infant walkers.
SeriousCPSCAug 6, 2026WURUI.BABY
BUSOHA magnetic fidget sliders recalled for magnet ingestion riskSold nationwide. BUSOHA magnetic fidget sliders contain loose magnets that can be easily removed from the silicone casing. If swallowed by a child, these high-powered magnets can attract each other or metal objects in the digestive system, causing serious injury or death through intestinal perforation, twisting, or blockage.
SeriousCPSCAug 6, 2026BUSOHA
Winston Porter and Seeday dressers recalled for tip-over riskSold nationwide. These wooden dressers can tip over and trap children if not anchored to a wall. One child was injured in a tip-over incident. The dressers don't meet federal safety standards for furniture stability.
SeriousCPSCAug 6, 2026Seeday
Louisville Ladder attic stairway ladders recalled for fall riskSold nationwide. The bolts on Louisville Ladder brand attic stairway ladders can break while in use, creating a fall hazard. The company has received 11 reports of bolts breaking, including one injury. This affects over 1.7 million ladders sold since 2012.
SeriousCPSCAug 6, 2026Louisville Ladder
DR Power PRO MAX30 mowers recalled for laceration riskSold nationwide. The blades on certain DR Power PRO MAX30 walk-behind lawn mowers can keep running even after you release the control lever, or may start spinning without the control being engaged. This creates a serious risk of cuts or lacerations. The manufacturer has received 19 reports of this problem but no injuries yet.
SeriousCPSCAug 6, 2026Generac
VMC compounded glutathione vials recalled for elevated endotoxinSold nationwide. Victory Medical Center Pharmacy identified elevated bacterial endotoxin levels in certain lots of its compounded glutathione 200 mg/mL multi-dose vials used for injection. Endotoxin contamination can cause serious reactions including fever, low blood pressure, severe headache, and in rare cases, anaphylactic shock or death. The pharmacy has received reports of adverse events from patients who received the product.
SeriousFDAAug 5, 2026Victory Medical Center Pharmacy
Hudson RCI neonatal breathing circuits recalled for connector overheatingSold nationwide. Medline Industries recalled Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits because the electrical connector at the Neptune humidifier can overheat, causing discoloration, melting, smoke, or burning. When this happens, the device automatically shuts off the heated wire function, which means infants may receive unheated or unconditioned breathing gas that can damage the airway and increase the risk of respiratory complications.
ModerateFDAAug 5, 2026Medline
DQ chocolate ice cream mix recalled for metal shavingsGalliker Dairy Co, Inc. is recalling DQ Chocolate Reduced Fat Ice Cream Mix (5-gallon containers) because metal shavings have been found in the product. The affected product was distributed in Pennsylvania, Delaware, New Jersey, Maryland, and New York.
ModerateFDAAug 5, 2026DQ
Mellish Island Super Skin supplement recalled for undeclared fishSold nationwide. Mellish Island Super Skin capsules contain marine collagen derived from fish, but the product label does not declare this fish ingredient. People with fish allergies who consume this supplement without knowing it contains fish could have an allergic reaction.
ModerateFDAAug 5, 2026Mellish Island
Fresenius Kabi Morphine syringes recalled for wrong opioid in packagingSold nationwide. Fresenius Kabi recalled one lot of Morphine Sulfate Injection 2 mg/1 mL prefilled syringes due to a labeling error. Packages labeled as morphine may actually contain Dilaudid (hydromorphone), a different and more potent opioid. Using the wrong medication could cause serious respiratory problems or death, especially in patients not used to opioids or those with lung disease.
SeriousFDAAug 4, 2026Fresenius Kabi