State

West Virginia product recalls

20,364 recalls have nationwide distribution and so reach West Virginia. 0 additional recalls listed West Virginia specifically in their distribution scope.

About recalls in West Virginia

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect West Virginia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14651–14675 of 20364

SevereFDA (Food)·F-0214-2023·2023-01-11
Cranberry Sweets Meltaway Recalled for Undeclared Peanut Allergen
Cranberry Sweets & More Inc is recalling Peanut Butter Meltaway chocolates mislabeled as Mint Meltaways. The product contains undeclared peanut, a major food allergen, posing risk to allergic consumers.
Product
Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read Mint Meltaways, Cranberry Sweets and more, Coos Bay, OR 97402. The back label is read Heirloom Mint Meltaways, Ingredients: Milk Chocolate (***soy lecit
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0797-2023·2023-01-11
Biomerieux VIDAS RUB IGG Tests Recalled Due to Storage Conditions
Biomerieux is recalling VIDAS RUB IGG diagnostic tests nationwide after storage temperature and duration exceeded specifications, affecting product performance guarantees.
Product
VIDAS CLINICAL VIDAS RUB IGG 60 TESTS, CATALOG 30226
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0815-2023·2023-01-11
Clinical reagent recalled due to temperature and time excursion
Biomerieux Inc is recalling VITEK MS CLINICAL REAGENT VITEK MS-CHCA due to temperature and time excursions that may prevent product performance guarantees. No illnesses reported.
Product
VITEK MS CLINICAL REAGENT VITEK MS-CHCA, CATALOG 411071
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0858-2023·2023-01-11
PPM Lombard TSA Neutralizer Culture Media Recalled for Storage Defect
Biomerieux is recalling 74 units of PPM Lombard Products TSA 3P neutralizer culture media due to temperature and time storage excursions. Product performance cannot be guaranteed.
Product
PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 423723
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0822-2023·2023-01-11
FDA Recalls ETEST Ertapenem Antibiotic Susceptibility Test Due to Storage Damage
Biomerieux Inc. is recalling ETEST Clinical Ertapenem antibiotic susceptibility test strips after temperature and time excursions compromised product performance. Affected units cannot guarantee accurate test results.
Product
ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0851-2023·2023-01-11
ETEST Clinical Eravacycline ERV test kit recalled for temperature storage excursion
Biomerieux is recalling ETEST Clinical Eravacycline ERV test kits nationwide after temperature and time storage conditions exceeded acceptable ranges, making product performance unreliable.
Product
ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0813-2023·2023-01-11
Culture Medium Recall Due to Temperature Excursion Affecting Product Performance
Biomerieux Inc recalls PPM INDUSTRY COMBOURG LPT BROTH culture medium batches 2117760 and 2120100 due to temperature excursion that may compromise product performance and reliability.
Product
PPM INDUSTRY COMBOURG LPT BROTH (4X3L), CATALOG 410849
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0792-2023·2023-01-11
VITEK 2 AST-GP67 Reagent Test Kit Recalled Due to Storage Condition Excursion
Biomerieux Inc. is recalling VITEK 2 Antibiotic Susceptibility Test Kits (AST-GP67) due to storage temperature and time conditions exceeding acceptable limits, which cannot guarantee product performance.
Product
VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0782-2023·2023-01-11
Beaver Surgical Eye Knife Recalled for Sterile Barrier Compromise
Beaver Visitec is recalling its surgical eye knife (Part 376630) used in cataract procedures due to compromised sterile packaging that may lead to infection. Approximately 599 units have been affected in the US.
Product
Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular paracentesis incisions in cataract procedures. Part Number: 376630
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0779-2023·2023-01-11
Steris Biological Indicators Recalled for Inconsistent Spore Growth
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because some units in lot 230613 fail to consistently promote spore growth, potentially masking failed sterilization cycles.
Product
VERIFY Dual Species Self-Contained Biological Indicators, 100 per box Item Number: S3061 Intended for use in installation testing and routine monitoring of steam and ethylene oxide sterilization processes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0828-2023·2023-01-11
ETEST Minocycline Susceptibility Test Affected by Storage Temperature Exceedance
Biomerieux is recalling ETEST CLINICAL MINOCYCLINE MC 256 clinical diagnostic tests nationwide due to storage temperature exceedance that may affect test performance and reliability.
Product
ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0831-2023·2023-01-11
ETEST Clinical Vancomycin Test Kits Recalled Due to Storage Damage
Biomerieux Inc is recalling 7 units of ETEST Clinical Vancomycin VA 256 test kits due to storage temperature excursions that may compromise test performance. Affected kits were distributed nationwide.
Product
ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0837-2023·2023-01-11
VITEK 2 Antibiotic Susceptibility Test Kits Recalled for Storage Condition Exceedance
Biomerieux is recalling VITEK 2 REAGENT AST-GN80 test kits due to temperature and time excursions during storage or handling. Product performance cannot be guaranteed for affected units.
Product
VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS, CATALOG 413437
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0812-2023·2023-01-11
FDA Recalls ASTUTE Electronic Quality Control Device for Storage Condition Excursion
Biomerieux Inc. is recalling ASTUTE electronic quality control devices due to temperature and time storage excursion that may compromise product performance in laboratory settings.
Product
ASTUTE REAGENT ASTUTE ELECTRONIC QUALITY CTRL DEVICE US, CATALOG 400016
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0840-2023·2023-01-11
Gene-Up Lysis Kit Recalled Due to Storage Condition Violations
Biomerieux Inc is recalling Gene-Up Lysis Kit (Catalog 414057) because storage conditions were exceeded and product performance cannot be guaranteed. Nationwide distribution.
Product
GENE-UP REAGENT GENE-UP LYSIS KIT, CATALOG 414057
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2023·2023-01-11
Programmable Diagnostic Computer Software Update Addresses Crash Errors
Siemens is updating software in 638 Programmable Diagnostic Computers distributed in the US to fix four software errors that could crash the device or corrupt password storage, potentially delaying diagnostics.
Product
Programmable Diagnostic Computer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0857-2023·2023-01-11
VITEK 2 AST-XN09 test kit recalled for improper storage temperature and time conditions
Biomerieux is recalling VITEK 2 AST-XN09 test kits where performance cannot be guaranteed due to storage outside proper temperature and time parameters. Affected kits nationwide should not be used.
Product
VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0794-2023·2023-01-11
FDA Recalls Reagent Nozzle Cleaning Solution Due to Storage Temperature Exceedance
Biomerieux Inc is recalling a reagent nozzle cleaning solution (Catalog 29588) because storage temperature and time conditions were exceeded, preventing product performance guarantee.
Product
PREVI COLOR GRAM REAGENT NOZZLE CLEANING SOLUTION (NA), CATALOG 29588
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0817-2023·2023-01-11
ETEST Amikacin Test Strips Recalled for Storage Condition Excursion
Biomerieux is recalling ETEST CLINICAL AMIKACIN AK 256 US S30 test strips (batch 1009209480) because temperature and time storage conditions were exceeded, and product performance cannot be guaranteed.
Product
ETEST CLINICAL AMIKACIN AK 256 US S30, CATALOG 412218
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0795-2023·2023-01-11
VIDAS Varicel Zoster IGG 60T Recalled Due to Storage Condition Excursion
Biomerieux Inc is recalling VIDAS Varicel Zoster IGG 60T (Catalog 30217, Batch 229478) due to storage temperature and time exceedance. The recalled units cannot be guaranteed to perform accurately.
Product
VIDAS CLINICALVIDAS VARICEL. ZOSTER IGG 60 T, CATALOG 30217
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0876-2023·2023-01-11
PPM Lombard Phosphate Buffer Recall Due to Temperature Exposure
Biomerieux Inc is recalling PPM Lombard Phosphate Buffer products due to temperature and time exposure during storage or transport that may have compromised product performance.
Product
PPM LOMBARD PRODUCTS T PHOSPHATE BUFFERSTERILE 20X9ML, CATALOG T8035
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0848-2023·2023-01-11
VITEK 2 Diagnostic Test Kit Recalled for Storage Parameter Exceedance
Biomerieux is recalling 39 units of a diagnostic test kit because storage temperature and time parameters were exceeded, which may affect test performance and reliability.
Product
VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS, CATALOG 420915
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0829-2023·2023-01-11
Clinical Diagnostic Device Recall: ETEST Rifampicin RI 32 Performance Degradation
Biomerieux Inc is recalling ETEST CLINICAL RIFAMPICIN RI 32 clinical diagnostic strips because temperature and time storage parameters were exceeded, and product performance cannot be guaranteed.
Product
ETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2023·2023-01-11
Steris Biological Indicator Lot May Fail to Detect Inadequate Sterilization
Steris Corporation is recalling 338 boxes of VERIFY Dual Species Biological Indicators (Lot #230613) because some units fail to promote spore growth as intended, risking false-negative sterilization test results.
Product
VERIFY Dual Species Self-Contained Biological Indicators, 50 per box Item Number: S3060 Intended for use in installation testing and routine monitoring of steam and ethylene oxide sterilization processes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0811-2023·2023-01-11
TEMPO Control Kit Reagents Recalled Due to Storage Temperature Excursion
Biomerieux is recalling TEMPO REAGENTS TEMPO CONTROL KIT (catalog 80000) due to storage conditions exceeding temperature and time limits, compromising product performance. Batch 1009477900 was distributed nationwide.
Product
TEMPO REAGENTS TEMPO CONTROL KIT , CATALOG 80000
Category
Medical Device
Distribution
Distributed nationwide