State

US Virgin Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46801–46825 of 73987

HighFDA (Devices)·Z-2729-2016·2016-09-14
Hospira Recalls Plum A+3 Infusion Pumps Due to Undersized Diaphragm
Hospira Inc. is recalling 357,778 Plum A+3 Infusion Pumps because an undersized fluid shield diaphragm may cause alarms and interrupt therapy.
Product
Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Infusion Systems are a multi-purpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self-contained, microprocessor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2738-2016·2016-09-14
Terumo Recalls Pinnacle Introducer Sheaths Due to Valve Leakage
Terumo Medical Corporation is recalling Pinnacle Introducer Sheaths due to a manufacturing issue causing valve leakage, which poses a risk of incremental blood loss.
Product
PINNACLE¿ Introducer Sheath PINNACLE PRECISION ACCESS SYSTEM¿ Sheath PINNACLE¿ TIF TIP" Introducer Sheath PINNACLE¿ R/O II Radiopaque Marker Introducer Sheath
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2762-2016·2016-09-14
Riverpoint Medical Recalls Webglo Polypropylene Surgical Sutures Due to Seal Issues
Riverpoint Medical is recalling specific lots of Webglo polypropylene surgical sutures because the seals may open during distribution or packaging.
Product
Polypropylene Surgical Sutures, brand Webglo, for vet use. Product is sterile. Part number: GP8665 Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2763-2016·2016-09-14
Blackrock NeuroPort Biopotential Signal Processing System Recall for Labeling Error
Blackrock Microsystems is recalling 81 Neural Signal Amplifiers because the device and patient cable are incorrectly labeled as Type CF Applied Parts.
Product
Neural Signal Amplifier. Part Numbers: 4208, 5703, 5749, 5748, 5747. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes. Biopotential signals include…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2074-2016·2016-09-14
Nature Made Hair Skin Nails Gummies Recalled for Microbial Count
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Product
Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC 0-31604-04132-8-1
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2764-2016·2016-09-14
Blackrock NeuroPort Patient Cables Recalled for Incorrect Labeling
Blackrock Microsystems is voluntarily recalling 120 Patient Cables because they are incorrectly labeled as Type CF Applied Parts.
Product
Patient Cable. Part Numbers: 4460, 6735. Sterile within Chipboard Boxes within corrugated cartons. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1491-2016·2016-09-14
Zydus Recalls Bromocriptine Mesylate Capsules Due to Stability Test Failures
Zydus Pharmaceuticals is recalling 14,808 bottles of Bromocriptine Mesylate 5 mg capsules because stability samples failed impurity tests.
Product
BROMOCRIPTINE MESYLATE — BROMOCRIPTINE MESYLATE (BROMOCRIPTINE MESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2742-2016·2016-09-14
Siemens ADVIA Centaur PSA Assay Recall for Clinical Interpretation Clarification
Siemens Healthcare Diagnostics is recalling ADVIA Centaur PSA Assay kits to emphasize that PSA values must be interpreted according to current clinical guidelines for biochemical recurrence.
Product
ADVIA Centaur¿ PSA Assay; Cat No. 06574155/SMN 10310292 (100 test)/02676506/SMN 10310293 (500 test)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2073-2016·2016-09-14
Nature Made Hair Skin Nails Gummies Recalled for Microbial Count
Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.
Product
Nature Made(R) adult gummies Hair.Skin.Nails, 90 count, UPC 0-31604-04016-1
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2747-2016·2016-09-14
Mentor Breast Tissue Expanders Recalled Due to Product Mix-Up
Mentor Texas, LP. is recalling 65 units of MENTOR CPX4 breast tissue expanders because a 350cc unit was found in a carton intended for 450cc units.
Product
MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1481-2016·2016-09-14
Amerisource Recalls Mispackaged Dextroamphetamine and Amphetamine Tablets
Amerisource Health Services is recalling 221 cartons of mixed amphetamine tablets due to unit dose mispackaging, where blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 5 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1494-2016·2016-09-14
Teva Recalls Argatroban Injection Due to Manufacturing Deviations
Teva North America is voluntarily recalling 1,299 bags of Argatroban Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL) , Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-0020-31 (Single Use Bag), NDC # 0703-0020-32 (5 Single Use Bags in One Carton).
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2743-2016·2016-09-14
Integra Recalls Achillon Suture System Due to Sterility Concerns
Integra LifeSciences is recalling the Achillon Suture System because internal studies suggest the secondary package seal may not maintain intended sterility.
Product
Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The Achillon Suture System is a single use, sterile device used to treat acute Achilles tendon ruptures. The Achillon Suture System is a mini-invasive procedure indicated to teat acute Achilles tendon…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2748-2016·2016-09-14
Mentor CPX4 Breast Tissue Expanders Recalled for Product Mix-Up
Mentor Texas, LP. is recalling 70 units of CPX4 breast tissue expanders because a 350cc product was found in a carton labeled for the 450cc version.
Product
MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2077-2016·2016-09-14
Nature Made Vitamin D Tablets Recalled for Yeast and Mold
Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.
Product
Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2075-2016·2016-09-14
Nature Made Vitamin D tablets recalled for yeast and mold
Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.
Product
Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2076-2016·2016-09-14
Nature Made Vitamin D Tablets Recalled for Potential Yeast and Mold
Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.
Product
Nature Made(R) D3 1000IU, 300 count, UPC 0-31604-02683-7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2759-2016·2016-09-14
Teleflex Horizon Manual-Load Ligating Clip Applier Recalled for Incorrect Etching
Teleflex Medical is recalling 49 units of Horizon Manual-Load Ligating Clip Appliers due to incorrect etching on the device.
Product
WECK¿ Horizon" Manual-Load Ligating Clip Applier, For Medium-Large Size Horizon Ligation Clips Curved Jaw, 11 (28cm), Rx Only, REF 337111, Product Usage: Weck Closure Systems applier has been designed and calibrated for use with specific Horizon, Hemoclip Plus Hemoclip…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1496-2016·2016-09-14
Teva Recalls Eptifibatide Injection Vials Due to Manufacturing Deviations
Teva North America is voluntarily recalling 14,661 vials of Eptifibatide Injection due to CGMP deviations. The recall covers lots distributed nationwide and in Puerto Rico.
Product
Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial, For Intravenous Use Only, Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-1179-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1490-2016·2016-09-14
Amerisource Recalls Mispackaged Adderall XR 30 mg Extended-Release Capsules
Amerisource Health Services is recalling 761 cartons of Adderall XR 30 mg capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1497-2016·2016-09-14
Teva Recalls Ondansetron Injection Vials Due to Manufacturing Deviations
Teva North America is recalling 13,223 vials of Ondansetron Injection USP due to CGMP deviations. The recall covers lots distributed nationwide and in Puerto Rico.
Product
Ondansetron Injection USP 40 mg/20 mL (2 mg/mL), Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454 NDC # 0703-7226-01 (20 mL- Multi-dose Vial), NDC # 0703-72263-03 (10 Multi-dose Vials per carton)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1480-2016·2016-09-14
Isomeric Pharmacy Recalls Methylprednisolone Acetate/Lidocaine Injection Due to Sterilization Issue
Isomeric Pharmacy Solution, LLC is recalling Methylprednisolone Acetate/Lidocaine HCl Injection because excessive sterilization time may cause difficulty resuspending particles.
Product
Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection, 10 mL multidose vial, sterile. Rx only. Compounded by Isomeric Pharmacy Solutions, Salt Lake City, UT 84109,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2739-2016·2016-09-14
GE Healthcare Recalls Centricity Enterprise Archive Software Due to Data Loss Risk
GE Healthcare is recalling Centricity Enterprise Archive software version 3.0.x due to a potential for data loss when the cache disk is nearly full.
Product
Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. Qualified system administrators install, monitor and maintain the system. DICOM devices (e.g. modalities, workstations) communicate with the archive using the DICOM protocol…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1488-2016·2016-09-14
Amerisource Recalls Mispackaged Adderall XR 20 mg Extended-Release Capsules
Amerisource Health Services is recalling 666 cartons of Adderall XR 20 mg capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules, CII 20 mg, 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2078-2016·2016-09-14
Nature Made Vitamin D Tablets Recalled for Yeast and Mold
Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.
Product
Nature Made(R) D3 1000IU, 350 count, UPC 0-31604-04070-3
Category
Drug
Distribution
Distributed nationwide