State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58926–58950 of 74011

HighFDA (Devices)·Z-1291-2014·2014-04-02
Teleflex Medical Recalls Non-absorbable Polyamide Surgical Sutures
Teleflex Medical is recalling 32,271 units of non-absorbable polyamide surgical sutures because they failed to meet minimum needle attachment strength requirements.
Product
Suture, Non-absorbable, Synthetic, Polyamide, Sterile, Rx only, Product Usage: Non-absorbable polyamide surgical suture is a non-absorbable, sterile, flexible thread prepared from long-chain aliphatic polymers Nylon 6 and Nylon 6,6 and is indicated for use in soft tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1283-2014·2014-04-02
Teleflex Vista Optical Bladeless Laparoscopic Access Port Recalled for Gas Leakage
Teleflex Medical is recalling Vista Optical Bladeless Laparoscopic Access Ports because gas leakage can delay or prevent the completion of laparoscopic surgeries.
Product
5/10/12 mm Weck¿ Vista" Optical Bladeless Laparoscopic Access Port, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1285-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Cone Open Access Devices
Teleflex Medical is recalling 55,521 Weck Vista Universal Cone Open Access devices due to reported gas leakage that may delay laparoscopic surgeries.
Product
5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1276-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Laparoscopic Ports Due to Gas Leakage
Teleflex Medical is recalling 55,521 Weck Vista Universal Laparoscopic Ports because they may leak insufflation gas, potentially delaying or complicating laparoscopic surgeries.
Product
Weck¿ Vista", Universal Laparoscopic Port, Size 5/10mmx100mm, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1280-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Laparoscopic Ports Due to Gas Leakage
Teleflex Medical is recalling 55,521 Weck Vista Universal Laparoscopic Ports because complaints were received regarding leakage of insufflation gas, which can delay surgical procedures.
Product
Weck¿ Vista" Universal Laparoscopic Port, Size 5/10/12mmx100mm, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1287-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Port
Teleflex Medical is recalling 55,521 units of the Weck Vista Universal Balloon Open Access Port due to reported gas leakage that may delay laparoscopic surgeries.
Product
5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1277-2014·2014-04-02
Teleflex Medical Recalls 10mm Weck Vista Cannula Due to Gas Leakage
Teleflex Medical is recalling 55,521 units of 10mm Weck Vista Cannula-only devices due to reported leakage of insufflation gas, which may delay laparoscopic surgeries.
Product
10mm Weck¿ Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1296-2014·2014-04-02
Teleflex Medical Recalls Silk Sutures Due to Needle Attachment Defect
Teleflex Medical is recalling 32,271 units of sterile silk sutures because they failed to meet minimum needle attachment strength requirements.
Product
Sutures, Non-absorbable, Silk, Sterile, Rx only, Product Usage: Natural non-absorbable silk surgical suture is a non-absorbable, sterile, flexible multifilament thread composed of an organic protein called fibroin. This protein is derived from the domesticated species…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1295-2014·2014-04-02
Teleflex Medical Recalls Steel Sutures Due to Needle Attachment Strength Defect
Teleflex Medical is recalling 32,271 units of non-absorbable steel sutures because they failed to meet minimum needle attachment strength requirements.
Product
Sutures, Non-absorbable, Steel, Monofilament and Multifilament, Sterile, Rx only, Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1281-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Laparoscopic Ports
Teleflex Medical is recalling 55,521 Weck Vista Universal Laparoscopic Ports due to reported gas leakage that may delay surgical procedures.
Product
Weck¿ Vista" Universal Laparoscopic Port, Size 5/10/12mmx125mm, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1292-2014·2014-04-02
Teleflex Medical Recalls Non-absorbable Surgical Sutures for Needle Attachment Defect
Teleflex Medical is recalling non-absorbable poly(ethylene terephthalate) surgical sutures because they did not meet minimum needle attachment strength requirements.
Product
Sutures, Non-absorbable, Synthetic, Polyethylene, Sterile, Rx only, Product Usage: Non-absorbable poly(ethylene terephthalate) surgical suture is a multifilament, non-absorbable, sterile, flexible thread prepared from fibers of high molecular weight, long-chain, linear…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1288-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 units of Weck Vista Universal Balloon Open Access Ports due to reported gas leakage that may delay laparoscopic surgeries.
Product
5/10 Weck¿ Vista" Universal Balloon Open Access Port Short Length (53mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1279-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Cannula Due to Gas Leakage
Teleflex Medical is recalling 5/10 mm Weck Vista Universal Cannulas because they may leak insufflation gas, potentially delaying laparoscopic surgeries.
Product
5/10 mm Weck¿, Vista" Universal Cannula, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1302-2014·2014-04-02
BioCardia Recalls Morph AccessPro Steerable Introducers Due to Particulate Risk
BioCardia, Inc. is recalling Morph AccessPro Steerable Introducers because particulates in the inner lumen could cause an embolic event.
Product
Morph AccessPro Steerable Introducer; 6F Introducer, 90 cm working length: Single use only. BioCardia, Inc. San Carlos, CA 94070 BioCardia Morph AccessPro is intended to provide a pathway through medical instruments cush as balloon dilation catheters, guidewires or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1286-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 units of Weck Vista Universal Balloon Open Access Ports due to reported gas leakage that may delay laparoscopic surgeries.
Product
5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length (70mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1271-2014·2014-04-02
Mevion S250 Proton Radiation Therapy System Recalled for Positioning Error
Mevion Medical Systems is recalling the S250 Proton Radiation Therapy System because a geometric positioning error can occur after rotational corrections are applied to treatment fields.
Product
MEVION S250, System, Radiation Therapy, Charged-Particle, Medical used for Proton Radiation Therapy Product Usage: Proton Radiation Therapy
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1294-2014·2014-04-02
Teleflex Medical Recalls Polyglycolic Acid Sutures for Needle Attachment Defects
Teleflex Medical is recalling 32,271 units of absorbable polyglycolic acid sutures because they failed to meet minimum needle attachment strength requirements.
Product
Sutures, Absorbable, Synthetic, Polyglycolic Acid, Sterile, Rx only, Product Usage: Non-absorbable polypropylene surgical suture is a monofilament, Non-absorbable, sterile, flexible thread prepared from long-chain polyolefin polymer known as polypropylene and is indicated…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1282-2014·2014-04-02
Teleflex Medical Recalls 12mm Weck Vista Cannula Due to Gas Leakage
Teleflex Medical is recalling 12mm Weck Vista Cannulas because they may leak insufflation gas, potentially delaying laparoscopic surgical procedures.
Product
12mm Weck¿ Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1289-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 Weck Vista Universal Balloon Open Access Ports due to gas leakage that may delay laparoscopic surgeries.
Product
5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length (70mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1306-2014·2014-04-02
Abbott i-STAT G3+ Cartridge Recall for Inaccurate Blood Gas Results
Abbott Point of Care is recalling i-STAT G3+ Cartridges (Lot N13183) because they may produce incorrectly elevated PCO2 and depressed pH results.
Product
i-STAT G3+ Cartridge pH, pCO2 and pO2 measurements are used in the diagnosis, monitoring and treatment of respiratory disturbances and metabolic and respiratory based acid-based disturbances.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1290-2014·2014-04-02
Teleflex Medical Recalls Weck Vista Universal Balloon Open Access Ports
Teleflex Medical is recalling 55,521 Weck Vista Universal Balloon Open Access Ports due to gas leakage that may delay laparoscopic surgeries.
Product
5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length (100mm), Product Usage: An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1274-2014·2014-04-02
Synthes Ulna Osteotomy System Drill Template and Saw Guide Recall
Synthes, Inc. is recalling 343 Drill Templates and Saw Guides for the Ulna Osteotomy System due to potential mechanical failure of connecting screws or K-wires.
Product
Drill Template and the Saw Guide for the Ulna Osteotomy System. Intended for fixation of fractures, osteotomies, nonunions, replantations, and fusions of small bones and small bone fragments, including osteopenic bone in the ulna.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1202-2014·2014-04-02
Siemens Artis Q X-ray Systems Recalled for Potential Tube Breakdown
Siemens is recalling 19 Artis Q and Artis Q biplane systems because a breakdown of the x-ray tube could result in loss of x-ray imaging during clinical operation.
Product
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1179-2014·2014-04-02
Hill Dermaceuticals Recalls Subpotent Fluocinolone Acetonide Topical Oil
Hill Dermaceuticals is recalling 4,142 bottles of Fluocinolone acetonide 0.01% Topical Oil because the active ingredient was found to be subpotent during routine testing.
Product
SETON PHARMACEUTICALS Fluocinolone acetonide 0.01% Topical Oil (Scalp Oil), 4 fl.oz., Rx only Manufactured by: Hill Dermaceuticals, Inc. For: Seton Pharmaceuticals NDC 13925-507-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1299-2014·2014-04-02
Bio-Rad D-10 Hemoglobin Testing System Software Recall
Bio-Rad is recalling D-10 Hemoglobin Testing Systems because the software may occasionally generate duplicate results with incorrect sample identifiers.
Product
D-10" Hemoglobin Testing System, Model number: 220-0220 Manufactured by: Bio-Rad Laboratories, Inc. 4000 Alfred Nobel Drive Hercules, CA 94545 The D-10 Hemoglobin Testing System is a single module designed for hemoglobin analysis in mid-volume laboratories. The D-10…
Category
Medical Device
Distribution
Distributed nationwide