West Virginia recalls
3,413 federal recalls affecting West Virginia in the last 12 months - 60 West Virginia-specific plus 3,353 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-04CPSCTomyNationwideBoon NURSH baby bottles recalled for choking hazard
The hard plastic outer shell on these bottles can bubble or peel, creating loose pieces of film-like plastic that a baby could choke on. The manufacturer has received 135 reports of this issue, though no injuries have been reported yet.
- 2026-06-04CPSCBroqixinNationwideBroqixin pool drain covers recalled for entrapment risk
Broqixin-branded pool drain covers do not meet federal safety standards and can trap swimmers underwater, creating a drowning hazard. The white plastic covers (Model 11064W, about 7.36 inches wide) were sold online through Amazon from January to April 2026.
- 2026-06-04CPSCGudook Outdoor SportsNationwideGudook bicycle helmets recalled for safety standard failure
Gudook-branded bicycle helmets (model KY-055) do not meet mandatory safety standards for impact protection. The helmets can fail to protect your head in a crash, creating a serious injury or death risk. Only helmets with batch number 202503 and manufacture date March 2025 are affected.
- 2026-06-04CPSCEicongNationwideCrenlux pool drain covers recalled for entrapment risk
Crenlux pool drain covers do not meet federal safety standards and can trap swimmers or bathers underwater, creating a serious drowning hazard. The white plastic covers, about 8 inches in diameter, were sold online through Amazon from June 2025 to March 2026.
- 2026-06-04CPSCTiny LandNationwideTiny Land play tents recalled for fiberglass fiber irritation risk
Tiny Land children's play tents contain fiberglass poles that can shed fibers, causing skin and eye irritation. The company has received eight reports of fiber shedding resulting in irritation. The tents were sold online from November 2025 through March 2026.
- 2026-06-04CPSCLittle Grape Land USNationwideLittle Grape Land nursing pillows recalled for suffocation risk
Little Grape Land nursing pillows sold on Amazon do not meet federal safety standards and can obstruct an infant's breathing. The U-shaped pillows, sold in various patterns between August 2025 and April 2026, pose a serious risk of suffocation during infant feeding or tummy time.
- 2026-06-04CPSCWyzeNationwideWyze Solar Cam Pan recalled for fire and burn risk
Wyze Solar Cam Pan security cameras can overheat and catch fire if installed incorrectly. The incorrect assembly instructions may lead users to accidentally puncture the lithium-ion battery's metal casing with a long, flat-head screw, causing the battery to rapidly overheat. The company has received reports of six cameras catching fire and exploding, with six consumers suffering minor burns.
- 2026-06-03FDA-DeviceMedlineClass IINationwideMedline medical kit recalled for wrong syringe type
Some Medline EYE TRAY-LF convenience kits (SKU DYNJ21627P) contain syringes labeled as tuberculin syringes on the box, but the actual syringes inside are insulin syringes. Using the wrong syringe type could lead to incorrect dosing.
- 2026-06-03FDA-DevicePhilipsClass IINationwidePhilips Allura imaging systems recalled for drive failure
Hard drives in Philips Allura X-ray imaging systems may degrade after six years of use, potentially causing loss of imaging capability, motorized movement, or data. Some systems may temporarily restore function after a restart.
- 2026-06-03FDA-DevicePhilipsClass IINationwidePhilips Azurion imaging systems recalled for hard drive failure
Hard drives in Philips Azurion imaging systems may degrade after six years of use, potentially causing loss of imaging capability. In some cases, the system may need to be restarted to restore function temporarily. Philips has identified this issue in multiple Azurion models used in medical facilities.
- 2026-06-03FDA-DeviceGEClass IINationwideGE ApexPro CARESCAPE Telemetry Server recalled for monitoring loss risk
GE HealthCare has identified a situation where the ApexPro CARESCAPE Telemetry Server (versions 5.0 and 6.0) can lose ECG and SpO2 monitoring data if the system loses network connection to the central monitoring station. This affects 14 units used in hospitals and clinical settings.
- 2026-06-03FDA-DeviceGEClass IINationwideGE HealthCare CARESCAPE Telemetry Server recalled for monitoring loss risk
GE HealthCare identified a rare condition in CARESCAPE Telemetry Server v5.0 and v6.0 where a persistent network communication failure at the central monitoring station can result in loss of ECG and SpO2 (heart rhythm and blood oxygen) monitoring. The problem occurs only when the system is in a "NO COMM" or "OFF NETWORK" state at the central station.
- 2026-06-03FDA-DeviceMedtronicClass IINationwideMedtronic brain stimulation adaptor kit recalled for labeling error
A limited number of Medtronic 2x4 Pocket Adaptor Kits (Models 64001 and 64002) were labeled with incorrect Use-By-Dates. The affected kits are used with deep brain stimulation systems to treat parkinsonian tremor. No injuries have been reported.
- 2026-06-03FDA-DeviceDevicorClass IINationwideDevicor HydroMARK breast biopsy markers recalled for labeling mismatch
Devicor Medical Products is recalling HydroMARK Breast Biopsy Site Marker Model 4010-02-15-T3 due to incorrect labeling on individual packages inside boxes. Some boxes labeled as T3 markers may contain packages labeled as T4 markers, which could lead to use of the wrong marker type during a breast biopsy procedure.
- 2026-06-03FDA-DeviceAbiomedClass INationwideAbiomed Impella Controller recalled for electrical and alignment faults
Certain Impella Controller (AIC) consoles contain electrical faults including alarm failures, power-path problems, and inaccurate motor sensing. Additionally, improper alignment between the purge cassette and motor drive can prevent the purge system from priming correctly, requiring users to switch to a backup console.
- 2026-06-03FDA-DeviceMedlineClass INationwideMedline spinal anesthesia kits recalled for quality issues
Medline distributed multiple spinal anesthesia and nerve block procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection made by Huons Co. The anesthetic was recalled due to quality concerns, including problems with microbiology testing data and reports that the medication may not work as expected.
- 2026-06-03FDA-DeviceHalyardClass IINationwideHalyard Purezero nitrile gloves recalled for chemical permeation failure
Halyard Purezero Ultraviolet Nitrile Exam Gloves in sizes XS through XL failed to meet chemical permeation performance standards, meaning they may not provide adequate protection against certain chemicals. This affects approximately 452,500 units distributed nationwide.
- 2026-06-03FDA-DeviceAbiomedClass INationwideAbiomed Impella Controller recalled for hardware defects
Abiomed identified that certain Automated Impella Controller (AIC) units have internal hardware issues that could affect device operation. These include cable and component positioning problems that may interrupt motor controls, cause startup failures, or prevent the device from booting properly. Abiomed is implementing hardware updates through its servicing process.
- 2026-06-03FDA-DeviceBolton MedicalClass INationwideBolton Medical RelayPro stent-graft recalled for deployment risk
The proximal clasp on Bolton Medical's RelayPro Thoracic Stent-Graft System may disconnect from the outer control tube during use. This disconnection could prevent the stent graft from being released properly from its delivery system. The FDA has issued a labeling update to inform physicians and hospitals of this potential issue.
- 2026-06-03FDA-FoodFly By JingClass IINationwideFly By Jing Creamy Sesame Noodles recalled for undeclared peanut
Fly By Jing Creamy Sesame Noodles (3.8 oz packets) may contain peanuts due to cross-contamination during production, even though peanuts are not listed on the label. This poses a serious risk to people with peanut allergies. The recall affects approximately 3,419 cases with best-by dates between October 15, 2026 and March 23, 2027.
- 2026-06-03FDA-DrugAbbVieClass IIINationwideAbbVie PRED MILD eye drops recalled for stability issue
AbbVie is recalling specific lots of PRED MILD (prednisolone acetate) eye drops because they failed stability testing. The affected product may not maintain its intended strength or safety over time. Two lots are involved, with an expiration date of August 2026.
- 2026-06-03FDA-DrugAVEVAClass IIINationwideAveva nicotine patches recalled for elevated impurities
AVEVA nicotine patches (14 mg) distributed by Rugby Laboratories have elevated levels of chemical impurities that exceed safety standards for shelf life. The issue was discovered during stability testing of specific lots. No injuries have been reported.
- 2026-05-29FDA-PRChampion FoodsNationwideMotor City Pizza Co. 5 Cheese Bread recalled for Salmonella risk
Champion Foods is recalling certain batches of Motor City Pizza Co. 5 Cheese Bread because a milk powder ingredient supplied by California Dairies may be contaminated with Salmonella. The contamination was found in the milk powder used to make the seasoning blend, though no illnesses have been reported so far.
- 2026-05-28FDA-PRBetter Weather ActivesNationwideBetter Weather Fix Elixir recalled for undeclared kratom
Better Weather Actives LLC is recalling all lots of Better Weather Fix Elixir 15 ml because the product may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl, which are kratom alkaloids. These substances can cause serious effects including nausea, vomiting, rapid heart rate, hallucinations, and in severe cases, respiratory depression or loss of consciousness.
- 2026-05-28CPSCHop ThangNationwideMainstays fabric dressers recalled for tip-over hazard
Mainstays 9-drawer fabric dressers sold at Walmart can tip over if not anchored to the wall, creating a risk of serious injury or death to children. The dressers do not meet federal safety standards for clothing storage units. About 165,000 units are affected.
- 2026-05-28CPSCAnzmtosnNationwideAnzmtosn fidget spinner balls recalled for battery ingestion risk
These glowing fidget spinner balls come with a mini flashlight that contains two small button cell batteries. The batteries are easy for children to remove and swallow. Swallowed button batteries can cause serious internal injuries and death.
- 2026-05-28CPSCMisco EnterprisesNationwideMisco Sports Light-Up Racket Set recalled for battery hazard
The battery compartment screw on these rackets does not stay attached when opened, allowing children to easily access button cell batteries inside the shuttlecock. Swallowed button cell or coin batteries can cause serious internal injuries, including chemical burns, and can be fatal.
- 2026-05-28CPSCGiantexNationwideGiantex lounge chairs recalled for amputation hazard
Giantex outdoor lounge chairs (model NP10025NY) have a pinch point that can trap and amputate fingers when the backrest is adjusted. One person has already lost a finger this way. About 1,155 chairs were sold online between August 2023 and October 2025.
- 2026-05-28CPSCTzumiNationwideTzumi SLF Sauna Blankets recalled for fire and burn hazards
Tzumi Electronics' SLF Sauna Blankets (model 30065TAR) can overheat during use, creating fire and burn risks. The company has received six reports of overheating, including five cases of minor furniture damage. About 3,600 units were sold through Target, Macy's, Snappy, and online from February 2025 through February 2026.
- 2026-05-28CPSCProudly American StoreNationwidePanasonic lithium coin batteries recalled for child ingestion risk
Panasonic-branded VL2020 lithium coin batteries sold online were packaged in clear plastic bags without child-resistant packaging or required warning labels. If swallowed, coin batteries can cause serious internal burns and death within hours.
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