State

US Virgin Islands product recalls

73,219 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 30
Most recent: 2026-09-23

Of the 177 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17701–17725 of 73396

HighFDA (Devices)·Z-0780-2023·2023-01-11
VERIFY Steam Test Pack Biological Indicators May Fail to Detect Sterilization Failure
Steris is recalling VERIFY Steam Test Packs because biological indicators in affected lots may fail to correctly monitor steam and ethylene oxide sterilization, potentially allowing failed sterilization to go undetected.
Product
VERIFY Steam Test Pack (20 Tests and 5 controls) Item Number: S3065 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-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-0793-2023·2023-01-11
Medical Diagnostic Reagent Recalled Due to Storage Temperature Damage
Biomerieux Inc is recalling PREVI COLOR GRAM diagnostic reagent (Catalog 29586) distributed nationwide because improper storage conditions may have degraded product performance.
Product
PREVI COLOR GRAM REAGENT IODINE-B (NA), CATALOG 29586
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
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
ModerateFDA (Devices)·Z-0855-2023·2023-01-11
Medical Device Reagent Recalled for Temperature Storage Condition Failure
Biomerieux Inc recalls GENE-UP Salmonella 2 reagent (Batch 1009407250) after storage temperature and time limits were exceeded, preventing performance guarantee.
Product
GENE-UP REAGENT GENE-UP Salmonella 2, CATALOG 423105
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0786-2023·2023-01-11
Diagnostic Test Kit Recalled Due to Exceeded Storage Conditions
Biomerieux Inc is recalling API STAPH 25 diagnostic test kits because storage conditions exceeded safe temperature and time parameters. Product performance cannot be guaranteed for the affected batch.
Product
API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0849-2023·2023-01-11
Microbiological susceptibility test strips recalled for temperature and time excursion
Biomerieux Inc. is recalling ETEST Clinical Imipenem Relebactam test strips (Catalog 420927) distributed nationwide because the product experienced temperature and time excursions during storage. The manufacturer cannot guarantee the product's test performance.
Product
ETEST CLINICAL IMIPENEM RELEBACTAM IPR US S30, CATALOG 420927
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0873-2023·2023-01-11
Medical device TSA culture medium recalled due to storage temperature excursion
Biomerieux Inc. is recalling PPM Lombard TSA culture medium nationwide due to storage temperature excursion. The product may not perform to specification.
Product
PPM LOMBARD PRODUCTS TSA 10PLT, CATALOG M1040
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0800-2023·2023-01-11
VIDAS Quality Control Product Recalled for Storage Condition Deviation
Biomerieux Inc is recalling VIDAS CLINICAL QCV-QUALITY CONTROL VIDAS 60T nationwide due to storage temperature and time deviations that prevent performance guarantee. Batch 1009351560 is affected.
Product
VIDAS CLINICAL QCV-QUALITY CONTROL VIDAS 60T, CATALOG 30706
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0864-2023·2023-01-11
VIDAS HCG 60 Clinical Test Kits Recalled for Exceeded Storage Conditions
Biomerieux Inc is recalling VIDAS HCG 60 test kits because storage conditions were exceeded, which cannot guarantee product performance. No illnesses or injuries have been reported.
Product
VIDAS CLINICAL VIDAS HCG 60 TESTS, CATALOG 30405-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0872-2023·2023-01-11
Biomerieux Culture Media Recalled Due to Temperature and Time Excursions
Biomerieux Inc is recalling diagnostic culture media because temperature and time storage conditions exceeded acceptable specifications, which means product performance cannot be guaranteed.
Product
PPM LOMBARD PRODUCTS CT&TI-TSA + L & P80 10PLT, CATALOG C6045-TI
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0802-2023·2023-01-11
CHROMID MRSA Culture Medium Recalled for Storage Temperature Exceedance
Biomerieux Inc is recalling PPM CLINICAL CHROMID MRSA 20 PLT diagnostic culture media (84 units) due to temperature and time exceedance during storage that may compromise product performance.
Product
PPM CLINICAL CHROMID MRSA 20 PLT US, CATALOG 43841
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0790-2023·2023-01-11
VITEK 2 BCL Test Kit recalled for storage condition violations
A batch of VITEK 2 Reagent BCL Test Kit from Biomerieux Inc is being recalled because storage conditions were exceeded, and product performance cannot be guaranteed.
Product
VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0803-2023·2023-01-11
PPM Clinical Chromid VRE Culture Media Recalled for Storage Excursion
Biomerieux is recalling PPM Clinical Craponne Chromid VRE culture media because storage conditions (temperature and time) exceeded specifications. Batch 1009540400 was distributed nationwide in the United States.
Product
PPM CLINICAL CRAPONNE CHROMID VRE 20 PLT US, CATALOG 43851
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0852-2023·2023-01-11
Medical Device Recall: ETEST Meropenem/Vaborbactam Due to Storage Temperature Excursion
Biomerieux is recalling 6 units of ETEST Meropenem/Vaborbactam susceptibility test kits (Batch 1008848690) distributed nationwide because they were stored outside specified temperature and time ranges, preventing guarantee of product performance.
Product
ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0863-2023·2023-01-11
ETEST Clinical Colistin Test Product Recalled Due to Storage Conditions
Biomerieux Inc is recalling ETEST Clinical Colistin diagnostic test products because storage conditions exceeded safe parameters, making product performance unreliable. Affected batches were distributed nationwide.
Product
ETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0844-2023·2023-01-11
Laboratory Culture Medium Recalled Due to Storage Condition Failure
Biomerieux Inc is recalling PPM Lombard Products IRR Count-Tact 3P Agar because storage conditions exceeded acceptable temperature and time parameters, potentially compromising product performance.
Product
PPM LOMBARD PRODUCTS IRR COUNT-TACT 3P AGAR 100 PLT, CATALOG 418049
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0842-2023·2023-01-11
PPM Clinical CHROMID MRSA diagnostic product recalled due to storage condition exceedance
Biomerieux Inc is recalling a batch of PPM Clinical CHROMID MRSA diagnostic medium (catalog 414524) after storage temperatures and timeframes exceeded specification, preventing performance guarantees.
Product
PPM CLINICAL CHROMID MRSA S AUREUS 20PLT US, CATALOG 414524
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0816-2023·2023-01-11
Clinical Reagent Vitek MS-FA Recalled Due to Storage Condition Violations
Biomerieux is recalling VITEK MS-FA clinical reagent due to storage condition violations that degrade product performance. The recall affects 29 units distributed nationwide.
Product
VITEK MS CLINICAL REAGENT VITEK MS-FA, CATALOG 411072
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0839-2023·2023-01-11
Biomerieux CHROMID CARBA Laboratory Product Recalled Due to Storage Condition Violations
Biomerieux Inc is recalling CHROMID CARBA laboratory products nationwide because storage conditions exceeded acceptable temperature and time ranges. The company cannot guarantee product performance.
Product
PPM INDUSTRY COMBOURG CHROMID CARBA US 20 PLT, CATALOG 414012
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0821-2023·2023-01-11
ETEST Ceftriaxone Antibiotic Test Strips Recalled for Storage Condition
Biomerieux is recalling ETEST Clinical Ceftriaxone test strips nationwide because storage temperature and time conditions were exceeded, which may affect product analytical performance.
Product
ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0791-2023·2023-01-11
VITEK 2 Reagent Test Kit Recalled Due to Storage Temperature and Time Exceedance
Biomerieux Inc is recalling VITEK 2 Reagent NH Test Kit units nationwide because they were stored outside proper temperature and time parameters. Product performance cannot be guaranteed.
Product
VITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS, CATALOG 21346
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0826-2023·2023-01-11
Levofloxacin ETEST Clinical Test Recalled for Improper Storage Conditions
Biomerieux Inc. is recalling 7 units of ETEST CLINICAL LEVOFLOXACIN LE 32 US S30 diagnostic test kits (Batch 1009240000) due to temperature and time storage condition violations that prevent guarantee of product performance.
Product
ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0806-2023·2023-01-11
Biomerieux BIOBALL B.SPIZIZENII culture products recalled for storage failure
Biomerieux is recalling BIOBALL B.SPIZIZENII NCTC 10400 (Catalog 56012) microbiological test cultures because storage temperature and time conditions were exceeded, and product performance cannot be guaranteed.
Product
BIOBALL B.SPIZIZENII NCTC 10400 550X20, CATALOG 56012
Category
Medical Device
Distribution
Distributed nationwide