Delaware recalls

1,888 federal recalls affecting Delaware in the last 12 months: 40 sold in Delaware plus 1,848 sold nationwide. From the CPSC, FDA, USDA and NHTSA.

Recent recalls

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  • AirClub convertible bassinets recalled for infant fall hazard

    Sold nationwide. AirClub convertible bassinets (model QX-831) have a defective attachment mechanism that creates a dangerous gap between the bassinet and adult bed mattress. Infants can fall through this opening, causing serious injury or death. About 110,400 units were sold online between October 2023 and December 2025.

    SeriousCPSCMar 26, 2026AirClub

  • Vive Health bed rails recalled for entrapment and asphyxiation risk

    Sold nationwide. Vive Health bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. Two deaths have been reported. The recall affects three models: Compact Bed Rail (LVA2009SLV), Bed Rail Collection V (LVA2097SLV), and Bed Rail model LVA1024 purchased on or before August 21, 2023.

    SeriousCPSCMar 26, 2026Vive Health

  • 4our Kiddies tip restraint kits recalled for tip-over risk

    Sold nationwide. 4our Kiddies plastic furniture straps (tip restraint kits) can break or degrade over time, allowing furniture to tip over and potentially trap or injure children or elderly people. The plastic brackets and cables fail to meet safety standards, and CPSC has received reports of at least 150 incidents where these straps broke, including three furniture tip-overs.

    SeriousCPSCMar 26, 20264our Kiddies

  • Nexgrill metal wire grill brushes recalled for ingestion risk

    Sold nationwide. Nexgrill grill brushes sold at Home Depot can shed small metal wire bristles that may stick to food or the grill surface. If swallowed, these bristles can cause serious internal injuries requiring surgery. The company has identified at least 68 cases where bristles detached, including five people who needed medical care.

    SeriousCPSCMar 26, 2026Nexgrill

  • Check your Datascope battery charger left bay

    Sold nationwide. Datascope's Battery Charging Station (Model 0998-00-0802) for Cardiosave IABP batteries has a protruding screw in the left bay that can prevent certain batteries from inserting fully and charging properly. The right bay works normally. This affects 28 units distributed in select U.S. states and international locations.

    FDAMar 25, 2026Datascope

  • Stop using Hologic Aptima HPV Assay kits

    Sold nationwide. Hologic's Aptima HPV Assay test kits (Master Lot 929785) may produce invalid results or false negatives, meaning they could fail to detect HPV infection. The affected kits were distributed to healthcare facilities in California, Florida, Iowa, Illinois, Missouri, North Carolina, New Mexico, Puerto Rico, and Tennessee.

    ModerateFDAMar 25, 2026Hologic

  • Stop using STA Liatest D-Di test kits

    Sold nationwide. Diagnostica Stago's STA Liatest D-Di blood test kits are giving inaccurate measurements for D-dimer (a marker used to help rule out blood clots). The kits are showing higher-than-actual results across all test ranges. These kits are used in hospital and reference laboratories on specific analyzer machines.

    ModerateFDAMar 25, 2026Diagnostica Stago

  • ConvaTec EsteemBody drainable pouch recalled for possible leaks

    Sold nationwide. ConvaTec's EsteemBody Drainable Pouch (model REF:423643, 10–45mm) may leak because of a manufacturing issue. The affected pouches have lot numbers 5K00011 or 5K00714 and have been distributed worldwide. No injuries have been reported.

    ModerateFDAMar 25, 2026ConvaTec3 products

  • Check your Leksell Gamma Knife serial number

    Sold nationwide. Elekta has recalled certain Leksell Gamma Knife Perfexion and Icon radiosurgery systems because an adapter component may not be properly aligned or locked in place. This could affect the accuracy of radiation delivery during treatment. No injuries have been reported.

    ModerateFDAMar 25, 2026Elekta

  • Check your Stryker Cub crib serial number

    Sold nationwide. Some Stryker Cub Pediatric Cribs sold in the USA are missing two warning labels on the access doors. This affects 590 cribs with specific serial numbers. No injuries have been reported.

    ModerateFDAMar 25, 2026Stryker

  • Check LeMaitre Vascular Artegraft Graft packaging

    Sold nationwide. LeMaitre Vascular is recalling one unit of Artegraft Vascular Graft (Model AG740) distributed in Illinois due to a labeling mix-up on the outer packaging. The product box was labeled with an incorrect lot number, which could cause confusion during clinical use. No injuries have been reported.

    ModerateFDAMar 25, 2026LeMaitre Vascular

  • Stop using Welch Allyn Vision Screener VS100

    Sold nationwide. The Welch Allyn Spot Vision Screener VS100 (software version 3.2.0.1) may display an unintended flickering screen due to a software issue. Flickering lights can trigger seizures in people who are photosensitive.

    ModerateFDAMar 25, 2026Baxter

  • Stop using Howmedica MICS3 Saw Attachment

    Sold nationwide. The external screws that secure the cover on the Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment may loosen during use and detach. This affects all units with part number 210490 distributed across the United States and several other countries. No injuries have been reported.

    ModerateFDAMar 25, 2026Howmedica Osteonics

  • GE Centricity Universal Viewer recalled for cybersecurity risk

    Sold nationwide. GE is recalling three versions of Centricity Universal Viewer software, a program that displays medical images, including mammograms. User login credentials may be exposed on the local workstation, which could let an unauthorized person affect system availability or manipulate data. The recall covers 2,405 affected units, and no injuries have been reported.

    ModerateFDAMar 25, 2026GE3 products

  • Stop using Abbott ID NOW flu test kit

    Sold nationwide. Abbott Diagnostics has recalled certain lots of the ID NOW Influenza A & B 2 test kit because they produce an unusually high number of invalid results compared to what the instructions say to expect. Invalid results mean the test does not give a clear positive or negative answer, requiring a retest.

    ModerateFDAMar 25, 2026Abbott

  • Blackwing beef and pork under alert for uninspected production

    Sold nationwide. Blackwing Organic Meats sold beef and pork products that were produced without required federal inspection and some bear false USDA inspection marks. These products may contain harmful bacteria, allergens, or other contaminants. The affected products were produced between April 2024 and March 2026 and shipped nationwide.

    SeriousUSDAMar 25, 2026Blackwing Organic Meats

  • Wawa milk pints recalled for foreign plastic contamination

    Wawa is recalling four 16 oz pint milk products sold in plastic bottles: Reduced Fat Milk 2%, Double Dutch Chocolate Milk, Cookies & Cream Milk, and Chocolate Low-fat Milk. Foreign plastic material was found on the fill line, so the milk may contain plastic pieces. The products were distributed in New Jersey, Maryland, Delaware, and Pennsylvania, and no injuries have been reported.

    ModerateFDAMar 25, 2026Wawa4 products

  • MID EAST Zaatar mix recalled for undeclared sesame, wheat

    Sold nationwide. MID EAST Jordanian Zaatar spice mix in 5 lb bags contains sesame and wheat that are not listed on the label. This product was distributed to bakeries for use in breads and pastries. People with sesame or wheat allergies could have a serious reaction if they consume products made with this spice mix.

    SeriousFDAMar 25, 2026MID EAST

  • Apotex brimonidine/timolol eye drops recalled for lack of sterility assurance

    Sold nationwide. Apotex Corp. is recalling specific lots of brimonidine tartrate/timolol maleate eye drops because the manufacturer cannot confirm the product was sterilized properly. The affected lots are VJ8599 (expires 09/30/2026) and VL1668 (expires 01/31/2027). No infections or injuries have been reported so far.

    ModerateFDAMar 25, 2026Apotex

  • Stop using Somerset Therapeutics dexamethasone injection

    Sold nationwide. Somerset Therapeutics is recalling one lot of dexamethasone sodium phosphate injection because testing found impurity levels above acceptable limits as the product approached its expiration date. The affected lot (A240421, expiring 07/31/2026) was distributed nationwide. No injuries have been reported.

    ModerateFDAMar 25, 2026Somerset Therapeutics

  • Strides Pharma children's ibuprofen recalled for foreign substance

    Sold nationwide. Strides Pharma Children's Ibuprofen Oral Suspension (100 mg per 5 mL) has been recalled because some bottles contain gel-like masses and black particles. The affected bottles are 4 FL OZ (120 mL) size with lot numbers 7261973A or 7261974A, expiring 01/31/2027. No injuries have been reported.

    ModerateFDAMar 25, 2026Strides

  • Shaman Botanicals White Vein tablets recalled for higher-than-labeled 7-OH

    Sold nationwide. Shaman Botanicals is recalling White Vein Advanced Alkaloids chewable tablets because testing found the active ingredient (7-hydroxymitragynine) is present in higher amounts than stated on the label. The label says 7.5 mg per serving, but the actual content is greater. No injuries have been reported.

    SeriousFDAMar 25, 2026Shaman Botanicals

  • Stop using Amneal Magnesium Sulfate IV bags

    Sold nationwide. One lot of Amneal Magnesium Sulfate in Water for Injection IV bags was found to contain the wrong medication—Tranexamic Acid—inside the packaging. This mix-up affects hospitals that received the product between late December 2025 and late February 2026. No patients have been harmed so far.

    SeriousFDAMar 24, 2026Amneal Pharmaceuticals

  • Aisstxoer adult bicycle helmets recalled for head injury risk

    Sold nationwide. Aisstxoer brand adult bicycle helmets sold on Amazon do not meet safety standards for impact protection and fit stability. If you crash while wearing one, the helmet may fail to protect your head, risking serious injury or death.

    SeriousCPSCMar 19, 2026Yxtdz Store

  • Amazon Basics camping pocket knives recalled for laceration risk

    Sold nationwide. The blade on Amazon Basics Camping Folding Pocket Knives can fail to stay closed, creating a risk of cuts. Amazon received one report of the blade opening unexpectedly, though no injuries have been reported so far.

    SeriousCPSCMar 19, 2026Amazon

  • Frigidaire gas ranges recalled for burn risk from oven ignition

    Sold nationwide. Certain Frigidaire gas ranges can have a delayed ignition in the oven's bake burner, which may cause a sudden flame burst and burn injuries. About 174,800 ranges are affected, sold between June 2025 and January 2026. Electrolux Group and the CPSC have received 62 reports of delayed ignition and 30 reports of burn injuries.

    SeriousCPSCMar 19, 2026Electrolux

  • Goregent infant walkers recalled for fall hazard risk

    Sold nationwide. Goregent-branded infant walkers sold on Amazon can fit through standard doorways and do not stop at the edge of stairs, creating a serious fall risk. About 90 walkers with model number 901 and a yellow production label dated November 2025 are affected. No injuries have been reported yet.

    SeriousCPSCMar 19, 2026Goregent

  • BUILT LUUM tumblers recalled for button battery ingestion risk

    Sold nationwide. BUILT brand LUUM light up tumblers can crack or break, exposing the button cell battery inside. Children can access and swallow these small batteries, which can cause serious internal burns, chemical injuries, or death. One child has already put a battery from one of these tumblers in their mouth.

    SeriousCPSCMar 19, 2026BUILT

  • Specialized Turbo Como SL e-bikes recalled for fall hazard risk

    Sold nationwide. Specialized electric bicycles in the Como SL line have forks that can develop small cracks over time, which may lead to fork failure and cause the rider to fall. The company has received one report of a fork failure but no injuries so far.

    SeriousCPSCMar 19, 2026Specialized

  • Tainoki Fine Furniture office chairs recalled for fall risk

    Sold nationwide. Tainoki Fine Furniture is recalling height-adjustable swivel office chairs sold at HomeGoods because the metal base can bend during use, creating a fall risk. The recall affects Noah, Owen, and Warren model chairs sold between August and December 2025. No injuries have been reported.

    ModerateCPSCMar 19, 2026Tainoki Fine Furniture

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