State

US Virgin Islands product recalls

73,806 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 178
Critical: 12
Severe: 39
Most recent: 2026-10-21

Of the 178 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 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44576–44600 of 73984

HighFDA (Devices)·Z-1120-2017·2017-02-08
Siemens IMMULITE PSA Kit Recall Due to Negative Bias Results
Siemens is recalling two lots of IMMULITE PSA kits because they produce negative bias results, potentially affecting prostate cancer screening accuracy.
Product
IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LK3PS1, SMN 10706293 (US Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1125-2017·2017-02-08
Covidien Nellcor SpO2 Forehead Sensor Recalled for Latex Labeling Error
FDA is recalling 7,453 units of the Covidien Nellcor SpO2 Forehead Sensor because the label incorrectly states the product is latex-free, while the headband contains latex.
Product
Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; The Covidien Nellcor¿ Forehead SpO2Sensor, model RS10, is indicated for use when continuous non-invasive arterial oxygen saturation and pulse rate monitoring are required for patients weighing more than 40 kg.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1129-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 252 Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The devices are used for breast tissue removal.
Product
Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0465-2017·2017-02-08
VistaPharm Recalls Methadone Hydrochloride Due to Potential Bacterial Contamination
VistaPharm is recalling Methadone Hydrochloride Oral Concentrate because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.
Product
METHADONE HYDROCHLORIDE — METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V078000·2017-02-08
Mercedes-Benz Recalls 2017 E300 Models Due to Shift Lever Module Defect
Mercedes-Benz is recalling 2017 E300 and E300 4Matic vehicles because a damaged shift lever module may prevent gear selection, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ E300
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1134-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 326 Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers units distributed in the US and several international countries.
Product
Intact Disposable Wands (part of the Intact System) 777-120: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1119-2017·2017-02-08
Siemens Recalls IMMULITE PSA Kits Due to Negative Bias
Siemens Healthcare Diagnostics is recalling IMMULITE PSA kits worldwide because patient samples show an average negative bias of approximately -22%.
Product
IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LKUP1, SMN 10380956 (OUS Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1130-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling 185 units of Intact Disposable Wands because the sterile barrier was breached, compromising sterility.
Product
Intact Disposable Wands (part of the Intact System) 900-115: 5 Pack 15mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1131-2017·2017-02-08
Medtronic Intact Disposable Wands Recalled for Sterility Compromise
Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 320 units distributed worldwide.
Product
Intact Disposable Wands (part of the Intact System) 777-115: 5 Pack 15mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0452-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures
Dr. Reddy's Laboratories is recalling Flucanazole 200 mg tablets nationwide due to failed dissolution specifications and stability issues.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0451-2017·2017-02-08
Dr. Reddy's Recalls Flucanazole Tablets Due to Dissolution Failures
Dr. Reddy's Laboratories is recalling Flucanazole 150 mg tablets because they failed dissolution specifications and 18-month stability testing.
Product
FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1109-2017·2017-02-08
Immuno-Mycologics Recalls Cryptococcal Antigen Lateral Flow Assay Due to False Positives
Immuno-Mycologics is recalling 630 units of the Cryptococcal Antigen Lateral Flow Assay because specific lots have lower specificity, leading to reported false positive results.
Product
Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1115-2017·2017-02-08
Zimmer Biomet Recalls Vanguard Total Knee System Femoral Components Due to Labeling Errors
Zimmer Biomet is recalling Vanguard Total Knee System femoral components because packaging labels may incorrectly identify the size or side of the implant.
Product
Vanguard Total Knee System Vanguard Open Box Femoral Components Item Number: 183100 Description: VNGD PS OPEN INTL FEM RT 55 Item Number: 183102 Description: VNGD PS OPEN INTL FEM-RT 57.5 Item Number: 183104 Description: VNGD PS OPEN INTL FEM RT 60 Item Number: 183106…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1117-2017·2017-02-08
Ortho-Clinical VITROS Na+ Slides Recalled for Potential Biased Results
Ortho-Clinical Diagnostics is recalling VITROS Na+ Slides because they may produce biased results if stored on the analyzer for 10 days after minimum warm-up.
Product
VITROS Na+ Slides, (UPN 10758750004812) For in vitro diagnostic use only. VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1118-2017·2017-02-08
Siemens Mammomat Inspiration Mammography Systems Recalled for Software Error
Siemens Medical Solutions USA is recalling 55 Mammomat Inspiration digital x-ray mammography systems due to a software error.
Product
Mammomat Inspiration full, field digital,system,x-ray,mammographic Product Usage: The Mammomat Inspiration system is intended for mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals. Mammographic images can be…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1427-2017·2017-02-08
Roland Manzanilla Olives Stuffed With Anchovies Recalled for Microorganisms
Roland Foods is recalling Manzanilla Olives Stuffed With Anchovies because FDA sampling found non-pathogenic Gram Positive Rods.
Product
Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES, DR. WT. 3 OZ. (85g), UPC Code: 41224714021 and Case UPC Code: 10041224714028, Item # 71402, PRODUCT OF SPAIN
Category
Food
Distribution
Distributed nationwide
HighCPSC·17732·2017-02-07
Sony Expands Recall of VAIO Laptop Battery Packs for Fire Hazards
Sony is expanding a recall of Panasonic lithium-ion battery packs used in VAIO laptops due to overheating risks that can cause burns and fires.
Product
Panasonic battery packs used in Sony Electronics laptop computers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V074000·2017-02-07
Cruiser RV Recalls 2016-2017 Boss Trailers Due to Furnace Exhaust Defect
Cruiser RV is recalling 2016-2017 Boss recreational trailers because a vertically-mounted furnace may have exhaust ports at the top, creating an unsafe operating condition.
Product
CRUISER RV — CRUISER RV BOSS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V073000·2017-02-03
Lamborghini Recalls 2012-2017 Aventador Models Due to Fuel Leak Fire Risk
Lamborghini is recalling 2012-2017 Aventador vehicles because gasoline may contact the exhaust system, increasing the risk of a fire.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V070000·2017-02-03
Volkswagen Recalls 2017 Jetta Vehicles Due to Engine Seizure Risk
Volkswagen is recalling 2017 Jetta vehicles with 1.4L engines because the engine block may be improperly cast, potentially causing the engine to seize and leading to a loss of vehicle control.
Product
VOLKSWAGEN — VOLKSWAGEN JETTA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V072000·2017-02-03
REV Recalls 2016-2017 Motorhomes Due to Fuel Leak Risk
REV Recreation Group is recalling 391 Holiday Rambler and Fleetwood motorhomes because a spring shackle bolt may puncture fuel components, creating a fire hazard.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER XE, STORM, VACATIONER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V071000·2017-02-03
Midwest All-Poly 3000 Series Recalled for Brake Light Switch Defect
Midwest Fire Equipment is recalling one 2017 All-Poly 3000 Series vehicle because the stop light switch may fail to illuminate brake lights, increasing crash risk.
Product
MIDWEST — MIDWEST ALL-POLY 3000 SERIES
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·17V068000·2017-02-02
Nissan Recalls 2002 Pathfinder and Infiniti QX4 for Air Bag Defect
Nissan is recalling 2002 Pathfinder and Infiniti QX4 vehicles because the front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Product
INFINITI — INFINITI, NISSAN QX4, PATHFINDER
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·17081·2017-02-02
Disney Recalls Mickey Mouse Nightlights Due to Fire Hazard
Walt Disney Parks and Resorts is recalling Happy Holidays! Mickey Mouse Nightlights because liquid can leak onto electrical outlets, posing a fire hazard.
Product
Happy Holidays! Mickey Mouse Nightlights
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V067000·2017-02-02
BMW Recalls 2011-2012 Models for Rear Driveshaft CV Joint Defect
BMW is recalling specific 2011-2012 models because the rear driveshaft CV joint may break, causing loss of propulsion and increasing crash risk.
Product
BMW — BMW 335I, Z4, 335D, 535I
Category
Vehicle
Distribution
Distributed nationwide