West Virginia recalls
3,404 federal recalls affecting West Virginia in the last 12 months - 42 West Virginia-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideElscint Cardial; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceHeartSineClass IINationwideHeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J
Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.
- 2025-10-29FDA-DeviceSedecalClass IINationwideFollow cleaning instructions for Sedecal X-ray equipment
Sedecal is reminding users that the MobileDiagnost wDR 2.2 mobile X-ray system is not water-resistant. Improper cleaning can damage the equipment and may affect its safety and performance. Users must follow the cleaning instructions in the equipment manual.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD Veritor Connect Software recalled for unauthorized access risk
Unauthorized actors accessed product service credentials used by some BD technical support teams. This creates a risk that diagnostic test data and system information could be accessed, changed, or made unavailable until BD updates these credentials.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD Phoenix M50 system recalled for unauthorized credential access
Unauthorized actors gained access to service credentials used by BD technical support teams to access the BD Phoenix M50 Automated Microbiology System. Until these credentials are updated, there is a risk that unauthorized individuals could access the system and view, modify, or disrupt patient data and system function.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD MAX System recalled for unauthorized credential access risk
Support service credentials for some BD MAX diagnostic systems were accessed by an unauthorized person. Until BD updates these credentials, there is a risk that someone could gain unauthorized access to the system and the data it contains.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD BACTEC 9120 system recalled for credential access risk
Unauthorized actors gained access to service credentials used by BD technical support teams for the BACTEC 9120 blood culture system. Until credentials are updated, there is a risk that unauthorized parties could access the system or associated patient data.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD BACTEC blood culture systems recalled for credential compromise
Unauthorized actors accessed service credentials used by BD technical support teams to maintain certain BACTEC blood culture instruments. This could allow unauthorized access to affected devices and the patient data they contain until BD updates these credentials.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD EpiCenter system recalled for unauthorized credential access
Service credentials used by BD technical support teams were accessed by an unauthorized person. Until BD updates these credentials, there is a risk that someone could gain unauthorized access to the system and its data.
- 2025-10-29FDA-DeviceMedlineClass IINationwideMedline saline flush syringes recalled for concentration issue
Medline Industries identified a limited quantity of prefilled saline flush syringes (0.9% Sodium Chloride Injection, USP, 10 mL) that may not contain the correct concentration of sodium chloride. The affected syringes were distributed nationwide in the US and Canada.
- 2025-10-29FDA-DeviceBaxterClass IINationwideWelch Allyn SureTemp Plus oral probe recalled for low temperature readings
Some Welch Allyn SureTemp Plus thermometer oral probes were incorrectly programmed with rectal probe settings. These affected probes may display temperatures that are lower than actual body temperature, which could delay treatment of fever or infection.
- 2025-10-29FDA-DeviceTandem Diabetes CareClass IINationwideTandem insulin pumps recalled for unexpected insulin dose risk
Tandem Diabetes Care insulin pumps (t:slim X2 and Mobi models) with certain software versions may deliver an unexpected automatic insulin correction dose when paired with a Dexcom G7 sensor. This could cause low blood sugar (hypoglycemia). The issue affects specific software versions: t:slim X2 versions 7.9.0.1 and 7.10.1, and Mobi version 7.9.0.1.
- 2025-10-29FDA-FoodMCI FoodsClass INationwideEgg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
- 2025-10-29FDA-FoodMCI FoodsClass INationwideCheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
- 2025-10-29FDA-FoodDemers FoodClass INationwideScott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak
- 2025-10-29FDA-FoodKrogerClass ISmoked Mozzarella Penne Salad, packaged in plastic containers with various weights, with UPC 227573-1XXXX (sold at deli service counters) or UPC 227573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fry's, Gerbes, King Soopers, Payless, Ralphs and Smith's
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
- 2025-10-29FDA-FoodKrogerClass IBasil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fry's, Gerbes, King Soopers, Payless, Ralphs and Smith's
Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
- 2025-10-29FDA-FoodGeorgia NutClass IINationwidetru fru Strawberries + Creme Freeze-Dried Fresh, retail pouch 3.4oz UPC 850048358249, 6 retail units per case
potential for metal in product
- 2025-10-29FDA-FoodGeorgia NutClass IINationwidetru fru Dark + White Chocolate Freeze-Dried Strawberries. 1.7oz retail pouch UPC 850048358331. 12 retail units per case. 3.4oz retail pouch UPC 850048358270. 6 retail units per case. 13oz retail pouch UPC 850048358379. 16 retail units per case.
potential for metal in product
- 2025-10-27USDAClass INationwideThrow out E.A. Sween pulled pork sandwiches
E.A. Sween Company is recalling approximately 127,887 pounds of Deli EXPRESS BBQ Pulled Pork sandwiches because they may contain pieces of plastic. The plastic came from barbecue sauce bottles used during production. The sandwiches were made between January 13 and October 15, 2025, and sold nationwide. No injuries have been reported so far.
- 2025-10-25USDAClass INationwideThrow out Hormel Fire Braised chicken products
Hormel Foods recalled over 4.8 million pounds of frozen chicken breast and thigh products sold to restaurants, hotels, and institutions because they may contain pieces of metal from production equipment. The metal came from a conveyor belt used during manufacturing. No injuries have been reported.
- 2025-10-24USDAClass INationwideThrow out Golden Island pork jerky
LSI, Inc. is recalling Golden Island Korean barbecue pork jerky because pieces of metal from the production conveyor belt may be mixed into the product. The affected jerky was sold at Costco and Sam's Club with "best by" dates from October 23, 2025, through September 23, 2026. No injuries have been reported.
- 2025-10-23CPSC3MNationwide3M Scotch Thermal Laminator recalled for overheating risk
The Scotch Thermal Laminator model TL909-50 may overheat during use, creating a burn hazard. This affects units sold between August 2024 and September 2025 with specific serial numbers. No injuries have been reported.
- 2025-10-23CPSCBealifeNationwideBealife 5-Drawer Dressers recalled for tip-over risk
These white dressers can tip over and trap children if not anchored to a wall. The dressers do not meet safety standards for furniture stability. About 410 units were sold on Amazon between June and August 2025.
- 2025-10-23CPSCScepterNationwideScepter B62 fuel containers recalled for flash fire risk
Scepter B62 dual-chamber fuel containers lack required flame-prevention devices and have non-child-resistant spouts, violating federal safety standards. These defects create a serious risk of flash fire, severe burns, and poisoning if children access the fuel.
- 2025-10-23CPSCPro RecycleNationwideScepter B62 fuel containers recalled for flash fire risk
Scepter B62 dual-chamber fuel containers lack safety devices required by law to prevent flash fires and have spouts that are not child-resistant. These defects pose risks of serious burns, poisoning, and death, especially to children.
- 2025-10-23CPSCJ & D BrushNationwideBio Ionic curling iron recalled for detaching barrel burn hazard
The barrel of the Bio Ionic One-Inch-Long Barrel Curling Iron can snap and detach during use, posing a burn risk. The company has received 258 reports of the barrel detaching, including six minor burn injuries.
- 2025-10-23CPSCOlympia ToolsNationwideOlympia Tools Pack-N-Stroll wagon recalled for entrapment risk
The Pack-N-Stroll utility wagon has an opening between the organizational tray and sidewall that can trap a child's head. The wagon also lacks a restraint system, which increases the risk of falls.
- 2025-10-23CPSCSauna360NationwideSauna360 Tylö saunas recalled for collapsing bench hazard
Sauna360's Tylö Halmstad and Kiruna Hybrid sauna rooms contain benches that can collapse without warning, creating a fall hazard. The company has received seven reports of bench failures, including one person with head and neck injuries.
- 2025-10-23CPSCCranach HardwareNationwideCranach Hardware tip restraint kits recalled for tip-over hazard
Cranach Hardware plastic furniture straps can break or degrade over time, causing furniture secured with them to tip over. The plastic brackets and cable ties do not meet safety standards. At least 115 incidents of breakage have been reported, including six furniture tip-overs, though no injuries have occurred yet.
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