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.

59626–59650 of 74011

HighFDA (Devices)·Z-0826-2014·2014-02-05
Navilyst Medical Recalls Port Kits Due to Sterilization Barrier Breach
Navilyst Medical is recalling 920 Port Kits with Access Infusion Sets due to a possible breach of the sterilization barrier. The devices were distributed nationwide.
Product
Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Number H965450140, Catalog Number 45-014; 2) 8F/SL/Titanium Ports/NF, Product Number H965450170, Catalog Number 45-017; 3) 6F/SL/Plastic Port/F, Product Number H965450200, Catalog…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0871-2014·2014-02-05
Spacelabs AriaTelemetry Transmitters Recalled for SpO2 Display Errors
Spacelabs is recalling AriaTelemetry transmitters because they may display SpO2 values when sensors are disconnected or failed.
Product
ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or neonatal patient populations in a hospital environment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0895-2014·2014-02-05
Synergetics Recalls Stiff 25ga Wide Field Endo Illuminator Due to Seal Failure
Synergetics Inc is recalling specific lots of Stiff 25ga Wide Field Endo Illuminators because faulty seals on the outer pouch could fail, compromising sterility.
Product
Stiff 25ga Wide Field Endo Illuminator, Synergetics, inc. length 7.5 ft, sterile / EO, 56.21.25PS. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0884-2014·2014-02-05
Synergetics Recalls 23ga Endo Illuminator Due to Faulty Seals
Synergetics Inc. is recalling 102 units of 23ga Endo Illuminator devices because faulty seals on the outer pouch could result in seal failure.
Product
23ga Endo Illuminator (Eckardt Trocar Compatible), Synergetics, inc., length 8.0 ft, sterile / EO, 56.02.23P Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1432-2014·2014-02-05
Lambs Farm Snowball Cookies Recalled for Undeclared Allergens
The Lambs Farm, Inc. is recalling Snowball Cookies because the labels fail to declare milk, soy, and wheat allergens.
Product
Snowball Cookies sold under the Lambs Farm brand and packaged in a white metal tin with a net weight of 1 lb.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0883-2014·2014-02-05
Synergetics Recalls 72 Sterile Ophthalmic Endo Illuminators Due to Seal Failure
Synergetics Inc. is recalling 72 sterile ophthalmic Endo Illuminators because faulty seals on the outer pouch could fail, potentially compromising sterility.
Product
Endo Illuminator, Synergetics, inc., 20ga, length 7.0 ft, sterile / EO, 56.02. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0874-2014·2014-02-05
Synergetics Recalls Stiff 25ga Chow Illuminated Pick Due to Seal Failure
Synergetics Inc. is recalling 44 units of Stiff 25ga Chow Illuminated Picks because faulty seals on the outer pouch could fail, compromising sterility.
Product
Stiff 25ga Chow Illuminated Pick (Dull), Synergetics, inc., length 8.0 ft, sterile / EO, 56.07.25PS. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0897-2014·2014-02-05
Synergetics 25ga Mid-Field Endo Illuminator Recalled for Seal Failure
Synergetics Inc is recalling 25ga Mid-Field Endo Illuminators because faulty seals on the outer pouch could fail, potentially compromising sterility.
Product
25ga Mid-Field Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.22.25P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0869-2014·2014-02-05
BD BACTEC FX Diagnostic Instrument Recalled for False Negative Results
Becton Dickinson & Co. is recalling 198 BD BACTEC FX instruments because a component may fail, causing false negative results in clinical specimens.
Product
BD BACTEC FX- Top Unit instrument, catalog number 441385, and Bottom Unit instrument, catalog 441386, available as a single or a stack configuration; Manufactured by BD Diagnostic Systems, 7 Loveton Circle, Sparks, MD 21152. The BD BACTEC FX instrument is designed for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0889-2014·2014-02-05
Synergetics Recalls 23ga Wide Field Corona Endo Illuminator Due to Seal Failure
Synergetics Inc is recalling 108 units of 23ga Wide Field Corona Endo Illuminators because faulty seals on the outer pouch could result in seal failure.
Product
23ga Wide Field Corona Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.12.23P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1436-2014·2014-02-05
Lambs Farm Blueberry Bread Recalled for Undeclared Soy Allergen
The Lambs Farm, Inc. is recalling Blueberry Bread loaves sold in Bread Trio gift boxes because the labels do not declare soy allergens.
Product
Blueberry Bread loaf sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 8 oz. This product was only sold as a part of the Bread Trio gift box.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0890-2014·2014-02-05
Synergetics Recalls 25ga Wide Field Corona Endo Illuminator Due to Seal Failure
Synergetics Inc is recalling 96 units of 25ga Wide Field Corona Endo Illuminators because faulty seals on the outer pouch could fail, compromising sterility.
Product
25ga Wide Field Corona Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.12.23P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1433-2014·2014-02-05
Lambs Farm Cookie Combo Recalled for Undeclared Milk and Wheat Allergens
The Lambs Farm, Inc. is recalling Cheerful Cookie Combo tins because the labels fail to declare milk and wheat allergens.
Product
Cheerful Cookie Combo containing an assortment of Lemon Butter Cookies and Famous Butter Cookies sold under the Lambs Farm brand and packaged in a white metal tin with a net weight of 1 lb.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0870-2014·2014-02-05
BD BACTEC FX 40 Diagnostic Instrument Recalled for False Negative Results
Becton Dickinson is recalling two BD BACTEC FX 40 instruments because a defective component may cause false negative results in clinical specimens.
Product
BD BACTEC FX 40 instrument, catalog number 442296, manufactured by BD Diagnostic Systems, 7 Loveton Circle, Sparks, MD 21152. The instrument is designed for the rapid detection of bacteria and fungi in clinical specimens. Samples are drawn from patients and injected directly…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0854-2014·2014-02-05
GE Healthcare Recalls CARESCAPE Patient Monitors Due to Safety Issues
GE Healthcare is recalling CARESCAPE B650 and B850 monitors due to 25 reported safety issues involving alarms and connectivity.
Product
GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. The CARESCAPE Monitor B650 is a multi-parameter patient monitor intended for use in multiple areas and intra-hospital transport within a professional healthcare facility. The CARESCAPE Monitor B650 is intended…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0855-2014·2014-02-05
Orthofix Firebird Modular Screw Driver Recalled for Collet Malfunction
Orthofix is recalling 443 Modular Screw Drivers because the collet may malfunction, preventing effective screw placement and delaying surgery.
Product
Orthofix Firebird Spinal Fixation System Instrumentation Modular Screw Driver, Product Usage: The Modular Screw Driver is used for inserting a modular bone screw into the pedicle during a spinal fixation procedure. It is a reusable instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V036000·2014-02-05
Peterbilt 567 and 579 Trucks Recalled for Missing Shifter Light Wiring
PACCAR is recalling 2014 Peterbilt 567 and 579 trucks because missing wiring may prevent the gear indicator from illuminating, increasing crash risk.
Product
PETERBILT — PETERBILT 579, 567
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0842-2014·2014-02-05
Biomerieux Recalls API Listeria Kits Due to ZYM B Reagent Defect
Biomerieux is recalling API Listeria kits because a defect in the ZYM B reagent may cause false negative results in biochemical tests.
Product
API Listeria (REF 10300) API Listeria is a standardized system for the identification of Listeria which uses miniaturized tests, as well as a database. The ZYM B reagent is including in API Listeria kit and it is used as an additional reagent for revealing the result of DIM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1042-2014·2014-02-05
Wockhardt Recalls Pantaprazole Sodium Tablets Due to Dissolution Failure
Wockhardt USA is recalling 1,129 bottles of Pantaprazole Sodium 40 mg tablets because they failed dissolution specifications.
Product
Pantaprazole Sodium Delayed Release Tablets , USP 40 mg, 1000 tablets bottle, Rx only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd Parsippany, NJ 07054 USA. NDC: 64679-0434-02.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0868-2014·2014-02-05
Siemens Free T3 Assay Kits Recalled for Positive Bias in Results
Siemens Healthcare Diagnostics is recalling Free T3 Assay kits due to a positive bias that may cause normal thyroid patients to appear abnormal.
Product
T3F, Free T3 Assay, REF/Catalog Number L2KF32 (200 tests), Siemens Material Number (SMN) 10381675, and REF/Catalog Number L2KF36 (600 Tests), SMN 10381682; an IVD Immunoassay kit for use with the IMMULITE 2000/IMMULITE 200 XPi Analyzers --- Origin: UK Siemens Healthcare…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0892-2014·2014-02-05
Synergetics Vivid Endo Illuminator Recalled for Faulty Sterile Seals
Synergetics Inc. is recalling Vivid Endo Illuminators because faulty seals on the outer pouch could fail, compromising the sterile status of the single-use ophthalmic devices.
Product
Vivid (tm) Endo Illuminator, 20ga, Synergetics, inc., length 7.5 ft, sterile / EO, 56.20P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0900-2014·2014-02-05
Boston Scientific Recalls 1068 Peripheral Imaging Catheters Due to Guidewire Issues
Boston Scientific is recalling 1,068 units of the Atlantis PV 8.5F Peripheral Imaging Catheter because physicians reported an inability to pass a guidewire through the device.
Product
Atlantis PV, 8.5F, 15 MHz Peripheral Imaging Catheter: Sterile, R; Sterilized using irradiation. Product Usage: This catheter is a 15 MHz ultrasound imaging catheter intended to operate with an IVUS instrument for diagnostic imaging. It is used with an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0825-2014·2014-02-05
Siemens ACUSON SC2000 Ultrasound System Recalled for Control Panel Lock Failure
Siemens is recalling 271 ACUSON SC2000 ultrasound systems because the control panel locking mechanism can fail, making the device difficult to steer during transport.
Product
ACUSON SC2000 Power Input: 100-240VAC, 1600 Max 50/60Hz; Siemens Medical Solutions USA, Inc. 685 East Middlefield Road Mountain View, CA 94043 Ultrasound imaging system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0867-2014·2014-02-05
Siemens Free T3 Assay Kits Recalled for Positive Bias in Results
Siemens Healthcare Diagnostics is recalling Free T3 Assay kits due to a positive bias that may cause normal thyroid patients to appear abnormal.
Product
T3F, Free T3 Assay, REF/Catalog Number LKF31, Siemens Material Number (SMN) 10381626; an IVD Immunoassay kit for use with the IMMULITE/IMMULITE 1000 Analyzers --- Shipping or unit package: 100, 200, 500 and 600 test kits --- Origin: UK Siemens Healthcare Diagnostics Products…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0840-2014·2014-02-05
GE Optima CT Systems Recalled for Manual Film Composer Data Mismatch
GE Healthcare is recalling 272 Optima CT520 and CT540 systems because the Manual Film Composer feature may display or print images with incorrect patient names or mismatched image previews.
Product
GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide