State

US Virgin Islands product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27426–27450 of 73754

SevereFDA (Devices)·Z-0030-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,262 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-14, Product Number: SVP2251, UDI: 20884521177380 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0024-2021·2020-10-07
blumen Clear Advanced Hand Sanitizer Recalled for CGMP Deviations
4e Brands North America is recalling blumen Clear Advanced Hand Sanitizer because it was manufactured in a facility associated with methanol contamination, representing poor Current Good Manufacturing Practices.
Product
blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL, (ethyl alcohol 70% v/v), Packaged as a) 2 fl oz / 60 ml bottle, UPC 8 14266 02371 6 b) 7.5 fl oz / 221 ml bottle, UPC 8 14266 02362 4 c) 15.2 fl oz (450 ml) bottle, UPC 8 14266 02392 1, d) 17 fl oz / 503 ml bottle with blue…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0049-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 9,214 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" C-13 Cutting SV2298, UDI: 20884521151021 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0034-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,811 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 1 Undyed 36" GS-25, Product Number: CV605, UDI: 20884521152295 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0023-2021·2020-10-07
Blumen Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk
4e Brands North America is recalling Blumen Advanced Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.
Product
blumen ADVANCED HAND SANITIZER, 70% ALCOHOL CONTENT, (70% ethyl alcohol), packaged as a) 3.4 fl oz / 100 ml bottle, UPC 8 14266 02359 4 b) 7.5 fl. oz./221 ml bottle, UPC 8 14266 02362 4 b) 33.8 fl. oz./1L bottle, UPC 8 14266 02369 3, Distributed in USA and Canada By: 4e Brands…
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3052-2020·2020-10-07
ESAOTE AC/DC Power Supply Recall for Portable Ultrasound Systems
ESAOTE is recalling AC/DC power adapters for specific portable ultrasound systems because the connector may heat up, smoke, or melt due to mechanical stress.
Product
AC/DC POWER SUPPLY for 7400, Part Number 151004300, XP Power Model Number AHM180PS19-XE0338, AC/DC Adapter associated with the following portable ultrasound diagnostic systems: The AC/DC adapter is intended for use with the following portable ultrasound systems: MyLabAlpha…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0002-2021·2020-10-07
Sun Pharmaceuticals Recalls RIOMET ER Due to NDMA Impurity
Sun Pharmaceuticals is recalling RIOMET ER (metformin hydrochloride) oral suspension because it contains the impurity NDMA.
Product
RIOMET ER (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL 16 oz. For Oral Use Only Rx Only Manufactured by: Sun Pharmaceuticals Industries Limited Mohali, India Distributed by: Sun Pharmaceuticals Industries, Inc. Cranbury, NJ 08512 NDC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0028-2021·2020-10-07
Modesa Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk
4e Brands North America is recalling Modesa hand sanitizer because it was manufactured in a facility associated with methanol contamination, representing poor manufacturing practices.
Product
Modesa instant HAND SANITIZER with moisturizers & vitamin E, (70% ethyl alcohol), 33.8 FL OZ (1 L) bottle, Distributed by Greenbrier International, Inc., 500 Volvo Parkway, Chesapeake, VA 23320, Made in Mexico. UPC 0 32251 49935 7
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1619-2020·2020-10-07
365 Organic Reduced Fat Popcorn Recalled for Glass Contamination
Eagle Family Foods is recalling 365 Organic Reduced Fat Popcorn because pieces of glass may be present in the product.
Product
365 Whole Foods Market Organic Reduced fat &Sodium Popcorn, 6 oz. bag, UPC 099482435349, 10 retail units per wholesale case
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0022-2021·2020-10-07
Blumen Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk
4e Brands North America is recalling Blumen Advanced Instant Hand Sanitizer due to manufacturing in a facility associated with methanol contamination.
Product
blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% Natural Boost with Tea Tree Oil, (70% ethyl alcohol), Packaged as a) 18 fl oz / 532 ml bottle, UPC 8 14266 02408 9 b) 33.8 fl oz / 1L bottle, UPC 8 14266 02374 7, Distributed in USA and Canada BY: 4e Brands…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0008-2021·2020-10-07
Endo GIA Stapler Recall Due to Incomplete Staple Formation
FDA recalls Endo GIA Auto Suture staplers because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Product
Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm, Item Code 030458 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0025-2021·2020-10-07
Blumen Aloe Hand Sanitizer Recalled for CGMP Deviations and Methanol Risk
4e Brands North America is recalling Blumen Aloe Advanced Hand Sanitizer because it was manufactured in a facility associated with methanol contamination, representing poor manufacturing practices.
Product
blumen Aloe ADVANCED HAND SANITIZER 70% ALCOHOL CONTENT (70% ethyl alcohol v/v), 3.4 fl. oz./100 mL bottle, Distributed in USA and Canada By: 4e Brands Northamerica LLC, 17806 IH-10W, Suite 300, San Antonio, Texas, 78257, Made in Mexico. UPC 8 14266 02358 7
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V618000·2020-10-07
Lamborghini Recalls 2020 Aventador SVJ Models for Suspension Bolt Issue
Lamborghini is recalling 2020 Aventador SVJ Coupe and Roadster vehicles because loose front suspension anchor bolts may cause a loss of vehicle control.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ ROADSTER, AVENTADOR SVJ COUPE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0044-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,266 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infections.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 18" P-12 Cutting SV497G, UDI: 20884521149707 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V621000·2020-10-07
Proterra Recalls 2019-2020 Catalyst Buses for Power Steering Hose Leak
Proterra is recalling 2019-2020 Catalyst buses because a power steering hose may leak fluid, increasing the risk of a crash.
Product
PROTERRA — PROTERRA CATALYST
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0033-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,276 units of Velosorb Fast Braided Absorbable Sutures because the product is non-sterile. This condition could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 36" KV-34, TaperCutting Product Number: CV916, UDI: 20884521153032 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0028-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Fast Braided Absorbable Sutures
Riverpoint Medical is recalling 1,248 units of non-sterile Velosorb sutures due to a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 5/0 Undyed 30" CV-23 Taper, Product Number: CV1213, UDI: 20884521150758 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0003-2021·2020-10-07
Endo GIA Stapler Recall Due to Incomplete Staple Formation
FDA is recalling Endo GIA Auto Suture Universal Articulating Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Product
Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm, Item Code 030452 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0012-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling non-sterile Velosorb sutures that could increase the risk of surgical site infections.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-12 Cutting, Product Number: SV426, UDI: 20884521151731 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21002·2020-10-07
Prestone Recalls Antifreeze for Child-Resistant Packaging Defects
Prestone is recalling about 687,000 antifreeze bottles because their caps may not engage the child-resistant mechanism, posing a poisoning risk to young children.
Product
Antifreeze products
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0017-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,258 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" P-24, Product Number: SV9911G, UDI: 20884521149776 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0016-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 3,110 units of non-sterile Velosorb sutures because they may compromise the sterile field and increase infection risk.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 18" P-14 Cutting, Product Number: SV6830, UDI: 20884521152349 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0023-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling non-sterile Velosorb Fast Braided Absorbable Sutures because they may compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 6/0 Undyed 30" P-10 Cutting, Product Number: SV4893, UDI: 20884521151717 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0047-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 7,982 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" CV-25 Taper CV3110, UDI: 20884521150918 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3026-2020·2020-10-07
Zeus ELISA Parvovirus B19 IgM Test System Recalled for False Positives
Zeus Scientific is recalling 74 units of the ZEUS ELISA Parvovirus B19 IgM Test System due to false positive results identified during an FDA inspection.
Product
ZEUS ELISA Parvovirus B19 IgM Test System, UDI 00845533001755 - Product Usage: intended for the qualitative detection of IgM class antibodies to human Parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human Parvovirus…
Category
Medical Device
Distribution
Distributed nationwide