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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Check Siemens Atellica CH A1c_E test resultsSold nationwide. Siemens has recalled certain lots of its Atellica CH A1c_E hemoglobin test kit because when used with another reagent (RCRP) on the same analyzer, the A1c test may give lower-than-accurate results. Lower results could delay diabetes diagnosis or lead to inadequate treatment. This issue does not affect labs using separate analyzers for each test.
ModerateFDAApr 8, 2026Siemens
- Check Paradise renal denervation catheter lot M4907
Sold nationwide. ReCor Medical distributed one Paradise ultrasound renal denervation catheter (Model PRDS-068-02, Lot M4907) that did not meet manufacturing standards and was supposed to be destroyed. The device was distributed in nine U.S. states. No injuries have been reported.
ModerateFDAApr 8, 2026ReCor Medical2 products
- Philips Trilogy Evo ventilators recalled for delayed alarm
Sold nationwide. Philips is recalling four Trilogy ventilator models running Software Version 1.05.15.00, covering 113,717 units in total. In some situations, the Obstruction Alarm does not sound within the time required by applicable standards and may take up to four breaths to trigger. No injuries have been reported.
SeriousFDAApr 8, 2026Philips4 products
- Abiomed Impella Controller recalled for possible delayed alarm
Sold nationwide. Abiomed's Impella Controller may display a delayed "Purge System Blocked" alarm when used with first-generation Impella 5.5 pumps. This could prevent timely detection of a blocked purge system. The issue affects 62 controllers with specific serial numbers in software versions 8.2.2 through 8.5.
SeriousFDAApr 8, 2026Abiomed
- Abiomed Impella Generation 1 purge cassettes recalled for leak risk
Sold nationwide. Abiomed is recalling purge cassettes used in Impella heart pump systems because Generation 1 cassettes have an increased risk of leaking during use. This affects multiple Impella pump models sold globally, with specific batch numbers identified from 2024.
SeriousFDAApr 8, 2026Abiomed
Mei Heong Yuen roasted peanuts recalled for banned cyclamatesSuper World Trading is recalling three flavors of Mei Heong Yuen roasted peanuts, all 9.17 oz (260g): tangerine, walnut and garlic. The FDA says the products contain cyclamates, a sweetener banned in the United States. No illnesses have been reported. The products were distributed in 19 states, including CO, CT, DE, FL, GA, IL, MA, MD, MI, NY, NC, NJ, OH, OR, PA, TX, UT, VA and WA.
ModerateFDAApr 8, 2026Mei Heong Yuen3 products
- Lone Star Dairy spray dried dairy powder recalled for Salmonella
Sold nationwide. Lone Star Dairy Products LLC is recalling spray dried milk powder products because Salmonella bacteria was found during testing of finished products. The recall affects specific lot codes of NFDM Low Heat, NFDM High Heat, and SMP Medium Heat products sold in 25 kg bags and 1 metric ton totes.
SeriousFDAApr 8, 2026Lone Star Dairy Products
- Cheetos and Loaded dumplings recalled for possible glass
JFE Franchising is recalling five dumpling products that may contain pieces of glass. The products are sold as Cheetos Flamin' Hot Loaded Dumpling, plus Dumpling Vegetable, Loaded Dumpling Vegetable and Dumpling Party Tray items. No injuries have been reported.
ModerateFDAApr 8, 2026JFE Franchising2 products
Divided Sunset collagen peptides recalled for undeclared egg and fishDivided Sunset Multi Collagen Peptides (8 oz pouch) contain egg and fish ingredients but do not clearly label them as allergens on the package. The ingredient list mentions eggshell membrane collagen and marine collagen but fails to state "EGG" or identify the fish species as required by law. This poses a risk to people with egg or fish allergies.
ModerateFDAApr 8, 2026Divided Sunset
Amneal magnesium sulfate IV bag recalled for tranexamic acid mix-upSold nationwide. Some cartons of Amneal Magnesium Sulfate IV bags were mislabeled and contained Tranexamic Acid (a different medication) instead. This mix-up affects lot AH250162 with an expiration date of 8/31/2027. The error was discovered before the product reached patients.
SeriousFDAApr 8, 2026Amneal Pharmaceuticals
- Appco Pharma prazosin capsules recalled for nitrosamine impurity
Sold nationwide. Appco Pharma LLC is recalling prazosin hydrochloride 1mg capsules (100-count bottles) because they may contain higher-than-acceptable levels of a nitrosamine impurity. This impurity was detected during manufacturing quality checks. The recall affects specific lot numbers distributed nationwide.
ModerateFDAApr 8, 2026Appco Pharma3 products
- Walgreens, Good Sense and more eye drops recalled for sterility
Sold nationwide. K.C. Pharmaceuticals is recalling eight sterile eye drop products because the company cannot confirm they are sterile. The drops were sold under store and pharmacy brands including Best Choice, Walgreens, GERI CARE, LEADER, Good Sense, Industrial Eye Relief and Rugby. No injuries have been reported.
ModerateFDAApr 8, 2026K.C. Pharmaceuticals8 products
- Amneal tramadol tablets recalled for impurity out of specification
Sold nationwide. Amneal Pharmaceuticals is recalling specific lots of tramadol 50 mg tablets because they contain higher-than-allowed levels of a chemical impurity called N-nitroso-desmethyl-tramadol (NDSRI). The impurity was discovered during stability testing of tablets nearing the end of their shelf life. No injuries have been reported.
ModerateFDAApr 8, 2026Amneal Pharmaceuticals
- Alembic bromfenac eye drops recalled for failed impurity testing
Sold nationwide. Alembic Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.07% because the medication failed purity and degradation tests during stability testing at 20 months. The affected eye drops may contain higher-than-acceptable impurity levels, which could affect safety and effectiveness.
ModerateFDAApr 8, 2026Alembic Pharmaceuticals
Good Brain Tonic recalled for potential botulismSold nationwide. Liquid Blenz Corp. is recalling all Good Brain Tonic beverages (16 oz and 32 oz bottles) due to a potential botulism risk. Botulism is a serious form of food poisoning. No illnesses have been reported yet, but the product was distributed nationwide.
SeriousFDAApr 6, 2026Liquid Blenz
Wawa Issues Product Recall on 16-oz. Wawa Brand Iced Tea Lemon, Iced Tea Diet Lemon, Diet Lemonade and Fruit Punch Due to Possible Undeclared Milk AllergenApril 3, 2026 Wawa, of Media PA, is recalling its 16 oz pints of Wawa Iced Tea Lemon, Wawa Iced Tea Diet Lemon, Wawa Diet Lemonade and Wawa Fruit Punch produced by the Wawa Beverage Company for sale in a limited number of Wawa stores located in Pennsylvania, Delaware, Maryland, New Jersey and Virgin
FDAApr 3, 2026
- RAW FARM raw cheddar cheese recalled for potential E. coli
Sold nationwide. Raw Farm has recalled specific batches of raw cheddar cheese products (blocks and shredded) due to a potential link to an E. coli O157:H7 outbreak. The recall includes multiple batch numbers and expiration dates listed on the Raw Farm website. No pathogens have been found in Raw Farm products tested so far.
SeriousFDAApr 2, 2026
Universal Broadmoor canopy bed frames recalled for collapse riskSold nationwide. The canopy beams on certain Samson International bed frames can collapse, especially when the bed is moved. The company has received five reports of the canopy collapsing and striking people, resulting in shoulder and head injuries.
SeriousCPSCApr 2, 2026Samson
Tuymec minoxidil hair spray recalled for child poisoning riskSold nationwide. Tuymec Minoxidil Hair Growth Spray bottles sold on Amazon do not have child-resistant caps, violating federal safety rules. Minoxidil is toxic if swallowed by young children and can cause serious injury or death.
SeriousCPSCApr 2, 2026DrHealBeauty
- Member's Mark children's pajama sets recalled for burn risk
Sold nationwide. Sam's Club is recalling Member's Mark Valentine-themed children's pajama sets because they don't meet mandatory flammability standards for sleepwear. This poses a risk of burn injuries. About 18,000 sets were sold online between December 2025 and January 2026.
SeriousCPSCApr 2, 2026Hansoll Textile
HTRC and Haisito T400 battery chargers recalled for fire riskSold nationwide. HTRC and Haisito brand T400 battery chargers can overheat and ignite, causing fires or explosions. The company has received 33 reports of fires and explosions, including three reports of injuries from burns and smoke inhalation.
SeriousCPSCApr 2, 2026Haitan
Sangohe bed rails recalled for entrapment and asphyxiation riskSold nationwide. Sangohe portable bed rails (models 504E and 504Q) can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 36,500 units were sold online starting August 2023.
SeriousCPSCApr 2, 2026Zhongshan KDB Health Solutions
- Granitestone Diamond Pro pans recalled for impact and burn hazards
Sold nationwide. The metal cap on the handle screw of these sauté pans can detach and eject forcefully when the pan is heated. E Mishan has received at least 98 reports of the cap detaching, including one case where a consumer was bruised and burned.
SeriousCPSCApr 2, 2026Mishan
TecFlox hair and beard serum recalled for child poisoning riskSold nationwide. TecFlox minoxidil topical solution bottles do not have child-resistant packaging as required by law. The liquid inside can cause serious injury or death if a young child swallows it. About 900 bottles were sold on Amazon in October 2025.
SeriousCPSCApr 2, 2026TecFlox
ELENKER portable bed rails recalled for entrapment and asphyxiation riskSold nationwide. ELENKER portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. The recalled models are silver collapsible rails sold on Amazon since August 2023.
SeriousCPSCApr 2, 2026Shiahaha
Ocun Condor HMS carabiners recalled for gate malfunction riskSold nationwide. OCUN NA is recalling certain Condor HMS Triple Carabiners sold from February 2025 through February 2026. The carabiner's gate can fail to close automatically and may require manual closing, which could cause the carabiner to fail during climbing and lead to a fall.
SeriousCPSCApr 2, 2026OCUN
Coluans Christmas light-up rings recalled for button battery ingestion riskSold nationwide. These Christmas light-up party favors contain button cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal burns and death. The rings were sold on Amazon between August and December 2025.
SeriousCPSCApr 2, 2026BUDI
Gavoyeat Halloween light-up rings recalled for battery ingestion riskSold nationwide. These Halloween light-up rings contain easily accessible button cell batteries that children can remove and swallow. Swallowed button batteries can cause serious internal burns and death within hours. About 800 units were sold on Amazon between June 2025 and January 2026.
SeriousCPSCApr 2, 2026CSZWEICD
Beestech spiral tower toys recalled for choking hazardSold nationwide. Beestech spiral tower toys sold on Amazon contain small plastic balls and are marketed for children under 3 years old, violating federal toy safety rules. The small balls pose a serious choking hazard. About 200 units were sold between November and December 2025.
SeriousCPSCApr 2, 2026Beestech
- Stop using Medline Puracol wound dressings
Sold nationwide. Medline Industries has recalled specific lots of Puracol and Puracol Plus collagen wound dressings due to elevated endotoxin levels. These contaminants can cause inflammation, tissue irritation, delayed healing, fever, low blood pressure, and in severe cases, septic shock.
SeriousFDAApr 1, 2026Medline
