State

US Virgin Islands product recalls

73,388 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 39
Most recent: 2026-09-23

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22301–22325 of 73565

ModerateFDA (Drugs)·D-0297-2022·2022-01-05
Betamethasone Dipropionate Lotion recalled for failed stability test
Teligent Pharma is recalling Betamethasone Dipropionate Lotion USP 0.05% (Augmented) due to failure to meet specification for the Active Pharmaceutical Ingredient particle test during routine stability testing.
Product
Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, Teligent Pharma Inc., Buena, NJ, 08310, NDC 52565-023-29
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0434-2022·2022-01-05
Medical Device FSH Test Substrate Error Causes Failed Tests and Delayed Results
bioMerieux is recalling VIDAS FSH test kits due to substrate errors that prevent the test from running, requiring repeated testing and delaying results.
Product
VIDAS FSH, REF 30407-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0436-2022·2022-01-05
VIDAS Lyme IgM II Diagnostic Test Kits Recalled for Substrate Error
bioMerieux is recalling three lots of VIDAS Lyme IgM II diagnostic test kits due to a substrate error that prevents the test from running, requiring users to conduct another test to obtain results.
Product
VIDAS Lyme IgM II (LYM), REF 416436
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0432-2022·2022-01-05
VIDAS RUB IgG Diagnostic Test Kit Recalled for Substrate Defect
bioMerieux is recalling three lots of VIDAS RUB IgG test kits due to substrate errors that prevent the test from running, potentially delaying diagnostic results.
Product
VIDAS RUB IgG (RBG), REF 30226
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0424-2022·2022-01-05
FDA Recalls VIDAS PRG Progesterone Test Kits for Substrate Error
bioMerieux is recalling 1,818 units of VIDAS PRG Progesterone test kits due to a substrate error that prevents the tests from running properly, causing delayed results when patients need repeat testing.
Product
VIDAS PRG Progesterone, REF 30409-01
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V002000·2022-01-04
LGS Industries Recalls 2014-2021 Trailers with Electric Rear Door Winch Defect
LGS Industries is recalling 2014-2021 trailers because the electric rear door winch cable may break, allowing the door to fall open and increasing injury risk.
Product
LGS INDUSTRIES — LGS INDUSTRIES PREMIER RACE, SHADOW, CARGO SPORT, JOURNEY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V001000·2022-01-01
Rosenbauer Fire Trucks Recalled for Fuel Tube Cracking and Fire Risk
Rosenbauer America is recalling 2018-2022 fire trucks because fuel tubes may crack, causing high-pressure leaks that could lead to fire.
Product
ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, COMMERCIAL 114SD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0288-2022·2021-12-29
Moxifloxacin 1 mg/mL Solution Label Mix-up Recall
Denver Solutions, LLC (doing business as Leiters Health) is recalling Moxifloxacin 1 mg/mL intracameral injection solution because vials labeled as 1 mg/mL may actually contain 5 mg/mL, creating a serious dosing error risk.
Product
Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0293-2022·2021-12-29
OTC Cough and Cold Drug Recalled for Microbial Contamination
Efficient Laboratories is recalling approximately 4,026 bottles of Rompe Pecho Max Multi-Symptoms cough and cold medicine nationwide due to potential microbial contamination of the non-sterile product.
Product
ROMPE PECHO MAX MULTI SYMPTOMS — ROMPE PECHO MAX MULTI SYMPTOMS (ACETAMINOPHEN, DEXTROMETHOPHAN HBR, PHENYLEPHRINE HCL, GUAIFENESIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0292-2022·2021-12-29
OTC Expectorant Recall: Microbial Contamination in Rompe Pecho
Efficient Laboratories is recalling Rompe Pecho guaifenesin expectorant in 4 fl oz and 6 fl oz bottles due to microbial contamination of non-sterile products. The affected product was distributed nationwide.
Product
ROMPE PECHO — ROMPE PECHO (GUAIFENESIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0311-2022·2021-12-29
NL Two-Bite Cream Cheese Iced Cinnamon Rolls Recalled for Potential Metal Contamination
GIVE AND GO is recalling NL two-bite Cream Cheese Iced Cinnamon Rolls nationwide due to potential metal contamination in the product.
Product
NL two-bite Cream Cheese Iced Cinnamon Roll 08030 16.93 lbs. case UPC 1-07-70981-08030-4
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0403-2022·2021-12-29
Hemashield Gold Knitted Bifurcated Vascular Graft Mislabeling Recall
Maquet Cardiovascular is recalling Hemashield Gold vascular grafts due to probable mislabeling. A different graft product may have been packaged in the carton.
Product
Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0302-2022·2021-12-29
GIVE AND GO Two-Bite Apple Caramel Cupcakes Recalled for Metal Contamination
GIVE AND GO is recalling two-bite apple caramel cupcakes (10 oz., UPC 770981055503) nationwide due to potential metal contamination in the product.
Product
two-bite apple caramel cupcakes 10 oz. UPC 7 70981 05550 3
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0401-2022·2021-12-29
Wright Medical CHARLOTTE MTP Hex Screw Recall: Incorrect Product in Packaging
Wright Medical recalled 22 units of CHARLOTTE MTP Hex Screws with incorrect product in packaging. Affected lots 02010697711582590 and 02010697711582591 were distributed to surgical facilities in the US, Canada, Australia, Spain, UK, and Chile.
Product
Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc Reconstruction System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0293-2022·2021-12-29
Give and Go Vanilla Cupcakes Recalled for Potential Metal Contamination
Give and Go is recalling two-bite vanilla cupcakes nationwide due to potential metal contamination in the product. Consumers should stop using affected units and contact the manufacturer.
Product
two-bite vanilla cupcakes 10 oz. UPC 7 70981 03460 7 Horneaditos cupcake de vainilla 10 oz. UPC 7 70981 04125 4
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0314-2022·2021-12-29
Favorite Day Bakery Frosted Sugar Cookies Recalled for Potential Metal
GIVE AND GO is recalling Favorite Day Bakery Frosted Sugar Cookies (13.5 oz., UPC 0 85239 41050 9) distributed nationwide due to potential metal contamination in the product.
Product
Favorite Day Bakery Frosted Sugar Cookies 13.5 oz. UPC 0 85239 41050 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0317-2022·2021-12-29
Kimberley's Bakeshoppe Sugar Cookies Recalled for Potential Metal Contamination
GIVE AND GO is recalling Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cookies (9.4 oz., UPC 7 70981 30310 9) due to the potential for metal in the product. The recall affects approximately 1,142,754 retail units distributed nationwide.
Product
Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cookies 9.4 oz. UPC 7 70981 30310 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0397-2022·2021-12-29
VirtuTRAX Instrument Navigator Sensor May Fail to Tighten Properly
Civco Medical Instruments is recalling VirtuTRAX Instrument Navigator sensors because they may fail to tighten properly onto surgical instruments. This functional defect could affect safe use during medical procedures.
Product
VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0291-2022·2021-12-29
Wondershop Vanilla Mini Cupcakes Recalled for Metal Contamination
GIVE AND GO is recalling Wondershop at Target vanilla mini cupcakes due to potential metal contamination in the product. Affected units were distributed nationwide.
Product
Wondershop at Target vanilla mini cupcakes 10 oz. UPC 0 85239 03474 3
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0402-2022·2021-12-29
Nurse Call Communication System Components May Fail to Reboot
Hill-Rom's NaviCare and Voalte nurse call communication systems may experience an unrecoverable software error causing components to fail reboot cycles and become non-functional, requiring replacement.
Product
These are communication systems, labeled as: a. NaviCare Nurse Call, Part Numbers: 3.6, 3.7, 3.9 b. Voalte Nurse Call, Part Number 4.0 *Product was rebranded from NaviCare to Voalte in 2020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0297-2022·2021-12-29
Cupcakes Recalled for Potential Metal Contamination
Two cupcake products sold nationwide are being recalled due to potential metal contamination. Affected consumers should stop consuming the products and contact the manufacturer for a refund.
Product
two-bite vanilla & chocolate cupcakes 20 oz. UPC 7 70981 03408 9 Favorite Day Bakery chocolate & vanilla mini cupcakes 10 oz. UPC 0 85239 12580 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0301-2022·2021-12-29
Pumpkin Spice Mini Cupcakes Recalled for Potential Metal Contamination
GIVE AND GO is recalling three brands of Pumpkin Spice mini cupcakes sold nationwide due to potential metal in the product. Consumers should not eat the affected cupcakes.
Product
Signature Select Pumpkin Spice mini cupcakes 10 oz. UPC 0 21130 98478 7 Bake Shop Pumpkin Spice mini cupcakes 10 oz. UPC 4 09910 02729 56 two-bite Pumpkin Spice cupcakes 10 oz. UPC 7 70981 05551 0
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0300-2022·2021-12-29
Carrot Cake Cupcakes Recalled for Potential Metal Contamination
GIVE AND GO is recalling two carrot cake cupcake products nationwide due to the potential presence of metal in the product. Consumers should not consume affected lots and should contact the manufacturer or return the product to the place of purchase.
Product
two-bite carrot cake cupcakes 10 oz. UPC 7 70981 05525 1 Kimberley's bakeshoppe carrot cake filled gourmet cupcakes 11.5 oz. UPC 7 70981 31026 8
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0412-2022·2021-12-29
Leica M220 F12 Surgical Microscope Optics Carrier May Drop Into Surgical Field
Leica Microsystems is recalling 2,800 M220 F12 surgical microscopes because the optics carrier may unintentionally drop into the surgical field, risking patient contact. No injuries have been reported.
Product
Leica Microsystems M220 F12 Microscope Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0295-2022·2021-12-29
Cupcakes Recalled for Potential Metal Contamination
GIVE AND GO is recalling approximately 1.14 million units of two-bite vanilla and chocolate cupcakes nationwide due to potential metal in the product.
Product
two-bite vanilla & chocolate cupcakes 10.5 oz. UPC 7 70981 03468 3 Sweet P's Bake Shop chocolate & vanilla cupcakes 10.5 oz. UPC 0 11225 54723 2
Category
Food
Distribution
Distributed nationwide