State

US Virgin Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33126–33150 of 73900

HighFDA (Devices)·Z-1933-2019·2019-07-10
Ortho-Clinical Diagnostics Recalls VITROS 250 Chemistry System for CK Drift
Ortho-Clinical Diagnostics is recalling 5,020 VITROS 250 Chemistry Systems due to potential negative drift in Creatine Kinase results.
Product
VITROS 250 Chemistry System, Product Code 8132086, (UDI # 10758750004409) Product Usage: Performs discrete clinical tests on serum, urine, and cerebral spinal fluid specimens. Methodologies include colorimetric (CM), potentiometric (PM), rate (RT), and immuno-rate (IR)…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19760·2019-07-10
Bose Recalls Commercial Loudspeakers Due to Falling Injury Hazard
Bose is recalling approximately 77,500 commercial loudspeakers because mounting components can break, causing the speakers to fall and pose an injury hazard.
Product
Professional use flush and surface mount loudspeakers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·19163·2019-07-10
Winco Recalls Black Cat Cat Mobile Fireworks Due to Explosion and Burn Hazards
Winco Fireworks is recalling Black Cat 'Cat Mobile' fireworks because the devices can burst and spread sparks upward and outward, posing explosion, burn, and projectile risks.
Product
Cat Mobile Fireworks
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1929-2019·2019-07-10
Philips Recalls Vereos PET/CT Systems Due to Cover Misalignment
Philips Medical Systems is recalling 70 Vereos PET/CT systems because misaligned covers may create gaps or protrude into the imaging bore.
Product
Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem images anatomical cross-sections by computer reconstruction of X-ray transmission data. The PET subsystem images the distribution of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1915-2019·2019-07-10
Siemens SOMATOM go.Up CT Scanner Recalled for Performance Issues
Siemens Medical Solutions is recalling nine SOMATOM go.Up CT scanners due to sporadic performance problems that may interrupt scanning workflows and delay patient diagnosis.
Product
SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1919-2019·2019-07-10
Siemens SOMATOM go.Up CT Systems Recalled for Performance Issues
Siemens is recalling 69 SOMATOM go.Up CT systems due to sporadic performance problems that may cause diagnostic delays or patient rescans.
Product
SOMATOM go.Up, Model No. 11061628 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1934-2019·2019-07-10
Ortho-Clinical Diagnostics Recalls VITROS 250AT Chemistry System
Ortho-Clinical Diagnostics is recalling 57 VITROS 250AT Chemistry Systems due to potential negative drift in Creatine Kinase (CK) test results.
Product
VITROS 250AT Chemistry System, Product Code 1758143, (UDI # 10758750000036) Product Usage: Performs discrete clinical tests on serum, urine, and cerebral spinal fluid specimens. Methodologies include colorimetric (CM), potentiometric (PM), rate (RT), and immuno-rate (IR)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1926-2019·2019-07-10
Infinium Medical Recalls CLEO and Tranquility VS Patient Monitors
Infinium Medical is recalling 95 CLEO and Tranquility VS patient monitors because their FDA clearance did not include the temperature monitor accessory option.
Product
CLEO Patient Monitor /Tranquility VS Patient Monitor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1916-2019·2019-07-10
Siemens SOMATOM go.Now CT Scanner Recall for Workflow Interruptions
Siemens Medical Solutions is recalling 53 SOMATOM go.Now CT scanners due to potential sporadic performance problems that may cause scanning workflow interruptions and delays in diagnosis.
Product
SOMATOM go.Now (Model #11061620), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1920-2019·2019-07-10
Siemens SOMATOM go.Now CT Systems Recalled for Performance Issues
Siemens is recalling 69 SOMATOM go.Now CT systems due to potential performance problems that may cause diagnostic delays or the need for patient rescans.
Product
SOMATOM go.Now, Model No. 11061618 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1946-2019·2019-07-10
Zimmer Biomet Recalls DVR Crosslock ePAK Screw Drivers Due to Packaging Seal Risk
Zimmer Biomet is recalling 3,022 DVR Crosslock ePAK Screw Drivers because sterile packaging seals may be weak, potentially compromising sterility.
Product
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1917-2019·2019-07-10
Siemens SOMATOM go.All CT Systems Recalled for Performance Issues
Siemens is recalling 24 SOMATOM go.All CT systems due to sporadic performance problems that may interrupt scanning workflows and delay diagnoses.
Product
SOMATOM go.All (Model #11061630), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1948-2019·2019-07-10
Zimmer Biomet Recalls K-Wire Trochar Tips Due to Packaging Seal Issues
Zimmer Biomet is recalling K-Wire Trochar Tips because the sterile packaging may have weak seals, potentially compromising the device's sterility.
Product
K-Wire Trochar Tip, Model Number 212000008 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1906-2019·2019-07-10
Bio-Rad Recalls EVOLIS Microplate System Due to Software Error
Bio-Rad is recalling 213 EVOLIS Microplate Systems because a software defect may cause erroneous test results to be transmitted to laboratory information systems.
Product
EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management Software, (Catalog no. 90471A.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1932-2019·2019-07-10
Medtronic Recalls 0-arm 1000 Imaging Systems Due to Charger Board Defect
Medtronic is recalling 832 0-arm 1000 Imaging Systems worldwide because a defective charger board prevents batteries from fully recharging, rendering the system inoperable.
Product
Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and B1-700-00028-XXX (where XXX indicates the system voltage): Product Name Model#/ CFN OARM ASSY 8170000027 SYSTEM PRODUCT BI70000027 OARM ASSY BI70000027R SYS PRODUCT RWK BI70000027R BASE OARM 8170000027100 SYSTEM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1454-2019·2019-07-10
InvaGen Recalls Testosterone Topical Solution Due to Defective Container
InvaGen Pharmaceuticals is recalling 1,776 bottles of Testosterone Topical Solution because defective containers may cause the actuator to function improperly, affecting dose delivery.
Product
TESTOSTERONE — TESTOSTERONE (TESTOSTERONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1947-2019·2019-07-10
Zimmer Biomet Recalls DVR Crosslock ePAK Depth Gauges for Packaging Defects
Zimmer Biomet is recalling DVR Crosslock ePAK Depth Gauges due to a potential for weak seals in the sterile packaging.
Product
DVR Crosslock ePAK Depth Gauge, Model Number 212000003 Product Usage: These DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1918-2019·2019-07-10
Siemens SOMATOM go.Top CT Systems Recalled for Performance Issues
Siemens Medical Solutions is recalling 30 SOMATOM go.Top CT systems due to potential performance problems that may interrupt scanning workflows and delay patient diagnoses.
Product
SOMATOM go.Top (Model #1161640), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1937-2019·2019-07-10
Beckman Coulter iChem VELOCITY Urine Strips Recalled for False Positives
Beckman Coulter is recalling iChem VELOCITY Urine Chemistry Strips because increased sensitivity causes falsely elevated urobilinogen results.
Product
iChem VELOCITY Urine Chemistry Strips, REF 800-7212, 100 test strips/vial. The firm name on the label is Beckman Coulter Ireland, Inc., Co. Clare, Ireland, Made in Germany.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1921-2019·2019-07-10
Siemens SOMATOM go.All CT Scanner Recalled for Performance Issues
Siemens is recalling 69 SOMATOM go.All CT scanners due to potential performance problems that may cause diagnostic delays or require patient rescans.
Product
SOMATOM go.All, Model No. 11061638 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1907-2019·2019-07-10
Phadia EliA RF IgM Well Recalled for Potential Low Assay Results
Phadia Ab is recalling EliA RF IgM Well kits due to a potential for reporting low assay results, which may affect rheumatoid arthritis diagnosis.
Product
EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measurement of IgM class rheumatoid factor antibodies in human serum and plasma (Li-heparin and EDTA) to aid in the diagnosis of rheumatoid arthritis in conjunction…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1922-2019·2019-07-10
Siemens CT System Recalled for Potential Scanning Workflow Interruptions
Siemens Medical Solutions is recalling 69 SOMATOM go.Top CT systems due to potential sporadic performance problems that may cause diagnostic delays or the need for patient rescans.
Product
SOMATOM go.Top, Model No. 11061648 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1438-2019·2019-07-10
Amneal Recalls Subpotent Esterified Estrogens and Methyltestosterone Tablets
Amneal Pharmaceuticals is recalling specific lots of Esterified Estrogens & Methyltestosterone tablets due to out-of-specification assay results.
Product
Esterified Estrogens & Methyltestosterone Tablets, USP 0.625 mg/1.25 mg, 100-count bottles, Rx Only, Manufactured by: Ammeal Pharmaceuticals of NY Hauppauge, NY 11788 Distributed by: Seton Pharmaceuticals Manasquan, NJ 08736, NDC 13925-171-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1927-2019·2019-07-10
Roche cobas p 501 Post-Analytical Units Recalled for Loose Flap
Roche Diagnostics is recalling four cobas p 501 post-analytical units because the tray input flap may become loose and detach from the instrument.
Product
cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1439-2019·2019-07-10
Amneal Recalls Subpotent Esterified Estrogens and Methyltestosterone Tablets
Amneal Pharmaceuticals is recalling specific lots of Esterified Estrogens & Methyltestosterone Tablets because they failed potency testing.
Product
Esterified Estrogens & Methyltestosterone Tablets, USP 1.25 mg/2.5 mg, 100-count bottles, Rx Only, Manufactured by: Ammeal Pharmaceuticals of NY Hauppauge, NY 11788 Distributed by: Seton Pharmaceuticals Manasquan, NJ 08736, NDC 13925-172-01
Category
Drug
Distribution
Distributed nationwide