State

US Virgin Islands product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30326–30350 of 73896

HighFDA (Devices)·Z-0891-2020·2020-02-05
Haemonetics Recalls Cell Saver 5/5+ Bowl Kits Due to Leak Risk
Haemonetics is recalling Cell Saver 5/5+ Bowl Kits because they may leak, trapping fluid and causing incomplete washing.
Product
Cell Saver¿5/5+ Bowl Kit (225 ml) Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0871-2020·2020-02-05
Zimmer Biomet Recalls ASI 2.0 Calcar Trimmer Shafts Due to Mating Failure
Zimmer Biomet is recalling 67 units of ASI 2.0 Calcar Trimmer Shafts because the shaft end may fail to mate effectively with the broach.
Product
ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0901-2020·2020-02-05
Haemonetics Recalls Cell Saver Bowl Sets Due to Potential Leaks
Haemonetics is recalling Cell Saver bowl sets because cracks may cause leaks and incomplete blood washing.
Product
Japan CS Elite FASTPACK DISP. SET - 125ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0847-2020·2020-02-05
Vitreq 25G Blunt and Brush Needles Recalled for Sterility Risk
Vitreq Bv is recalling VitreQ 25G Blunt and Brush Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
(1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G BF Brush Needles-BF25.D52 GTIN: 8719214221188
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0910-2020·2020-02-05
Collagen Matrix Recalls GIBSON Membrane Due to Incorrect Instructions
Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane Extended because they may have been packaged with incorrect Instructions for Use.
Product
GIBSON Healthcare Membrane Extended, 15mm x 20mm, Reference Number 5303-306 - - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0909-2020·2020-02-05
Collagen Matrix Recalls GIBSON Membrane Due to Incorrect Instructions
Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane 6-9 because they may have been packaged with incorrect Instructions for Use.
Product
GIBSON Healthcare Membrane 6-9, 30mm x 40mm, Reference Number 5303-299 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0883-2020·2020-02-05
Synthes 2.4mm Sterile Locking Screw Recall Due to Packaging Defect
Synthes is recalling 25 units of 2.4mm sterile locking screws because the inner packaging cap may open prematurely, potentially preventing the screw from being used during surgery.
Product
2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE, Part Number 04.210.124TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0882-2020·2020-02-05
Synthes Recalls 2.4mm Sterile Locking Screws Due to Packaging Defect
Synthes, Inc. is recalling 25 units of 2.4mm sterile locking screws because the inner packaging cap may open or fail to separate, potentially delaying surgery.
Product
2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE, Part Number 04.210.118TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0881-2020·2020-02-05
Synthes Recalls 2.4mm Sterile Locking Screws Due to Packaging Defect
Synthes, Inc. is recalling 25 units of 2.4mm sterile locking screws because the inner cap may open or the tube may remain in the outer cap, preventing screw removal.
Product
2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE, Part Number 04.210.116TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0907-2020·2020-02-05
Collagen Matrix Recalls GIBSON Membrane Due to Incorrect Instructions
Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane 6-9 because they may have been packaged with incorrect Instructions for Use.
Product
GIBSON Healthcare Membrane 6-9, 15mm x 20mm, Reference Number 5303-226 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0908-2020·2020-02-05
GIBSON Healthcare Membrane Recalled for Incorrect Instructions for Use
Collagen Matrix Inc is recalling GIBSON Healthcare Membrane 6-9 units because they may have been packaged with incorrect Instructions for Use.
Product
GIBSON Healthcare Membrane 6-9, 20mm x 30mm, Reference Number 5303-235 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets; localized…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0874-2020·2020-02-05
GE Healthcare Recalls SIGNA Premier MRI Systems Due to Date Errors
GE Healthcare is recalling 62 SIGNA Premier MRI systems because a potential installation issue could cause incorrect dates to be recorded on medical images.
Product
SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0912-2020·2020-02-05
GIBSON Healthcare Membrane Extended Recalled for Incorrect Instructions for Use
Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane Extended because they may have been packaged with incorrect Instructions for Use.
Product
GIBSON Healthcare Membrane Extended, 30mm x 40mm, Reference Number 5303-342 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0823-2020·2020-02-05
Macleods Pharma Recalls Montelukast Sodium Chewable Tablets for Dissolution Failure
Macleods Pharma USA is recalling 10,680 bottles of Montelukast Sodium Chewable Tablets, 5 mg, because testing revealed low out-of-specification dissolution results in one lot.
Product
MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0911-2020·2020-02-05
Collagen Matrix Recalls GIBSON Membrane Due to Incorrect Instructions
Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane Extended because they may have been packaged with incorrect Instructions for Use.
Product
GIBSON Healthcare Membrane Extended, 20mm x 30mm, Reference Number 5303-324 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0879-2020·2020-02-05
Synthes Recalls 2.4mm Sterile Locking Screws Due to Packaging Defect
Synthes, Inc. is recalling 25 units of 2.4mm sterile locking screws because the packaging may fail to keep the screw accessible, potentially delaying surgery.
Product
2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE, Part Number 04.210.110TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0880-2020·2020-02-05
Synthes Recalls 2.4mm Sterile Locking Screws Due to Packaging Defect
Synthes, Inc. is recalling 25 units of 2.4mm sterile locking screws because the packaging may fail to keep the screw sealed, potentially causing surgical delays.
Product
2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE, Part Number 04.210.112TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0859-2020·2020-02-05
Vitreq Bv Recalls VitreQ 23G Blunt Needles Due to Sterility Risk
Vitreq Bv is recalling VitreQ 23G Blunt Needles because microscopic tears in the sterile pouch may compromise sterility.
Product
VitreQ 23G Blunt Needles with luer-lock connector-REF: CN23.D05 GTIN: 8719214221621
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0875-2020·2020-02-05
GE Healthcare Recalls SIGNA Architect MRI Systems Due to Date Errors
GE Healthcare is recalling SIGNA Architect MRI systems because a potential installation issue may cause incorrect dates to be recorded on medical images.
Product
SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0877-2020·2020-02-05
GE Healthcare Recalls MRI Systems Due to Potential Date Setting Error
GE Healthcare is recalling 62 MRI systems because a potential installation issue may cause incorrect dates to be recorded on medical images.
Product
SIGNA Vibrant Nuclear Magnetic Resonance Imaging System, 1.5T Signa HDx, 1.5T Signa HDxt, Signa HDi - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0919-2020·2020-02-05
Arthrex Fibulock Fibular Nail Instrument Set Recalled for Potential Blockage
Arthrex, Inc. is recalling 47 units of the Fibulock Fibular Nail Instrument Set due to a potential for blockage of the Hub Attachment Tube.
Product
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0824-2020·2020-02-05
FDA Recalls Nystatin Oral Suspension for Subpotent Assay Levels
Pharmaceutical Associates Inc. is recalling Nystatin Oral Suspension because it failed potency testing at 12 months. Patients should stop using the product and consult their healthcare provider.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0876-2020·2020-02-05
GE Healthcare Recalls SIGNA Pioneer MRI Systems Due to Date Errors
GE Healthcare is recalling 62 SIGNA Pioneer MRI systems because an installation issue may cause incorrect dates on medical images.
Product
SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20E003000·2020-02-04
Cummins Recalls PowerDrive EV Drivetrains for Loss of Drive Power
Cummins is recalling PowerDrive EV drivetrains for school buses, step vans, and medium-duty trucks because a connector may unplug, causing sudden loss of drive power and power steering.
Product
POWER TRAIN recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V061000·2020-02-04
Hyundai Recalls Vehicles Due to ABS Module Fire Risk
Hyundai is recalling specific Elantra, Elantra Touring, Santa Fe, and Entourage models because moisture in the ABS module can cause an electrical short and engine compartment fire.
Product
HYUNDAI — HYUNDAI SANTA FE, ENTOURAGE, ELANTRA, ELANTRA TOURING
Category
Vehicle
Distribution
Distributed nationwide