State

US Virgin Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29051–29075 of 73774

HighFDA (Devices)·Z-1879-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Bleeding Risk
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1882-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175930P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1899-2020·2020-05-13
Varian Multileaf Collimator Recall Due to Software-Related Leaf Movement Failure
Varian Medical Systems is recalling 151 Multileaf Collimators because a software upgrade caused leaves to fail to move during specific arc treatments.
Product
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf Collimator Model Number(s): product code: H54 and H56; MLC software version 8.5 - Product Usage: is intended to assist the clinician in the delivery of external…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1841-2020·2020-05-13
Philips Recalls Transesophageal Ultrasound Transducers Due to Temperature Measurement Failure
Philips Ultrasound Inc is recalling S7-3t transesophageal transducers because a manufacturing programming error prevents the system from correctly measuring tip temperature, which may stop auto-cooling and cause patient injury.
Product
Transducer S7-3t UDI (01)00884838061439 REF 989605406772 Can be used with: CX50, EPIQ 7, Affiniti 50 and Affiniti 70 Ultrasound systems - Product Usage: Diagnostic ultrasound imaging or fluid flow analysis of the human body - particularly transesophageal echocardiography…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1838-2020·2020-05-13
Ivoclar Vivadent recalls dental ceramic blocks due to cracking during sintering
Ivoclar Vivadent AG is recalling 332 units of IPS e.max ZirCAD ceramic blocks because they crack during the sintering process. The recall covers lots Y47472 and Z000V0 distributed nationwide.
Product
Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - ceramic for dental use,intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized zirconium oxide blocks for the CAD/ CAM technology Product Number: 686194
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175728AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1259-2020·2020-05-13
Sandoz Recalls Infuvite Pediatric Injection Due to Defective Container Crimping
Sandoz is recalling 17,500 units of Infuvite Pediatric Multiple Vitamins Injection due to sub-optimal crimping in the vial. The product was distributed nationwide.
Product
INFUVITE PEDIATRIC — INFUVITE PEDIATRIC (MULTIPLE VITAMINS INJECTION)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1856-2020·2020-05-13
Nobel Biocare Universal Base Abutments Recalled for Incorrect Screws
Nobel Biocare is recalling 238 Universal Base CC RP 1.5 mm abutments because they may contain incorrect screws that could loosen.
Product
Universal Base CC RP 1.5 mm; The Universal Base Abutment in combination with Nobel Biocare end osseous implants are indicated for single-unit if screw retained and for multiple-unit if cement retained crowns are used; catalog no. 38214 - Product Usage: Dental implant abutments…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1857-2020·2020-05-13
Nobel Biocare Recalls Dental Implant Abutments Due to Incorrect Screws
Nobel Biocare is recalling 478 Temporary Snap Abutments because packages may contain incorrect screws that could loosen, requiring retightening.
Product
Temporary Snap Abutment Engaging CC RP 1.5 mm; Pre-manufactured prosthetic components directly connected to the endosseous implant; catalog no. 38761 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1853-2020·2020-05-13
Nobel Biocare Recalls Dental Implant Abutments Due to Incorrect Screw Risk
Nobel Biocare is recalling 239 units of Temporary Abutment Engaging CC RP components because packages may contain incorrect screws that could loosen.
Product
Temporary Abutment Engaging CC RP pre-manufactured prosthetic components directly connected to the endosseous implant, catalog no. 36664 - - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1927-2020·2020-05-13
ICU Medical Recalls Cogent Hemodynamic Monitoring System Due to Software Defect
ICU Medical is recalling 123 units of the Cogent Hemodynamic Monitoring System because a software issue prevents the system from storing patient IDs and information.
Product
The Cogent Hemodynamic Monitoring System. REF58400-000, GTIN 00840619099459; REF 58400-000R, GTIN 0087709094314; REF 58403, GTIN 00840619079505; REF 58401, GTIN 00840619079499 - Product Usage: intended for patients for whom the monitoring of continuous cardiac output and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1892-2020·2020-05-13
Trilliant Surgical Recalls 3.5mm Aresenal Screw Drill Bits Due to Labeling Error
Trilliant Surgical, LLC is recalling 3.5mm Aresenal Screw Drill Bits due to a labeling error where the lot number is incorrectly marked, potentially impacting device traceability.
Product
3.5mm Aresenal Screw Drill Bit , Ref: 330-35-001, Qty. 70, Rx Only, Non-Sterile, UDI: (01)00812926029696 - Product Usage: A drill bit facilitates implant insertion
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1845-2020·2020-05-13
TeDan Recalls Fukushima Suction Tubes Due to Incorrect Raw Material
TeDan Surgical Innovations LLC is recalling Fukushima suction tubes because incorrect raw material was used in production. The affected units were distributed in New Jersey.
Product
Fukushima suction tubes; Fukushima Malleable Tapered Suction, 3 FR, 145 MM; REF: TK-1110 - Product Usage: TSI Fukushima Suction Tubes are nonpowered, hand-held reusable manual surgical instruments for general use intended to be used in various general surgical procedures. They…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1839-2020·2020-05-13
Ivoclar Vivadent recalls dental ceramic blocks due to cracking during sintering
Ivoclar Vivadent AG is recalling 639 units of IPS e.max ZirCAD ceramic blocks because they crack during the sintering process.
Product
Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental use, intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized zirconium oxide blocks for the CAD/ CAM technology Product Number: 686195
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1910-2020·2020-05-13
Gentell Honey Hydrogel Recalled for FDA Registration Deficiency
Gentell, Inc. is recalling Gentell Honey Hydrogel because the product was not properly registered with the FDA, as discovered during an audit.
Product
Gentell Honey Hydrogel Hydrogel 4oz. Tube. Wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number: GEN-11340 - Product Usage: Use Gentell Honey Hydrogel on wounds with little or no exudate, diabetic skin ulcers, venous stasis ulcers, first and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1852-2020·2020-05-13
Nobel Biocare Recalls Dental Implant Abutments Due to Incorrect Screw Risk
Nobel Biocare is recalling 236 units of temporary dental implant abutments because packages may contain an incorrect screw that could loosen.
Product
Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components directly connected to the endosseous implant, catalog no. 36662 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1850-2020·2020-05-13
Epimed RF Injector Cannula Recalled for Incorrect Expiration Date Labeling
Epimed International is recalling 701 units of R-F Injector Cannulas due to incorrect expiration dates on the packaging. The devices were distributed worldwide and across multiple US states.
Product
R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124; REF/UDI: 257-2010D(01)00818788022127 - Product Usage:The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1854-2020·2020-05-13
Nobel Biocare Recalls Dental Abutments Due to Incorrect Screw Risk
Nobel Biocare is recalling 227 Esthetic Abutment CC RP 1.5 mm units because they may contain incorrect screws that could loosen.
Product
Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components directly connected to the endosseous implant, catalog no. 36669 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to restore…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1883-2020·2020-05-13
Northgate Technologies Recalls 9 FR AUTOLITH Probes for Biocompatibility Testing Failure
Northgate Technologies is recalling 9 FR AUTOLITH probes because a lot failed biocompatibility testing. The recall covers 298 boxes distributed nationwide.
Product
Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmentation of urinary/renal and biliary calculi.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1924-2020·2020-05-13
Wright Medical Recalls Inbone Tibial Trays Missing Plasma Coating
Wright Medical Technology Inc is recalling 22 units of Inbone Tibial Trays because one lot is missing the required plasma coating.
Product
WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient limited mobility by reducing pain, restoring alignment and replacing the flexion and extension movement in the ankle joint.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1908-2020·2020-05-13
Gentell Honey Hydrogel Gauze Recalled for FDA Registration Failure
Gentell, Inc. is recalling 22,439 units of Gentell Honey Hydrogel 4"x4" Saturated Gauze because the product was not properly registered with the FDA.
Product
Gentell Honey Hydrogel 4"x4" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number: GEN-11430 - Product Usage: Use Gentell Honey Hydrogel on wounds with little or no exudate, diabetic skin ulcers, venous stasis ulcers…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1909-2020·2020-05-13
Gentell Honey Hydrogel Saturated Gauze Recalled for FDA Registration Failure
Gentell, Inc. is recalling 4,348 units of Gentell Honey Hydrogel Saturated Gauze because the product was not properly registered with the FDA.
Product
Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number: GEN-11830 - Product Usage: Use Gentell Honey Hydrogel on wounds with little or no exudate, diabetic skin ulcers, venous stasis ulcers…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1907-2020·2020-05-13
Gentell Honey Hydrogel Gauze Recalled for FDA Registration Failure
Gentell, Inc. is recalling 85,586 units of Gentell Honey Hydrogel 2"x2" Saturated Gauze because the product was not properly registered with the FDA.
Product
Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing containing hydrogel and honey (100% Leptospermum honey), Model Number:GEN-11230 - Product Usage: Use Gentell Honey Hydrogel on wounds with little or no exudate, diabetic skin ulcers, venous stasis ulcers…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1849-2020·2020-05-13
Epimed RF Injector Cannula Recalled for Incorrect Expiration Date
Epimed International is recalling 1,374 units of RF Injector Cannulas due to incorrect expiration dates on the packaging.
Product
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 - Product Usage: The Epimed RF Introduction Cannula is intended for use in radiofrequency (RF) heat lesion procedures for the relief of pain.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V266000·2020-05-12
Blue Bird Recalls School Buses Due to Air Conditioner Fire Risk
Blue Bird is recalling 2020-2021 Vision and All American school buses because an incorrectly installed air conditioning circuit breaker may increase the risk of a fire.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide