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.

21576–21600 of 73565

HighFDA (Devices)·Z-0701-2022·2022-03-09
Helix Elite Molecular Standards recalled due to shelf life test failure
Microbiologics Inc is recalling Helix Elite Molecular Standards for Inactivated Influenza A/B and Respiratory Syncytial Virus because shelf life testing failed at 24 months, potentially affecting product stability.
Product
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Influenza A/B and Respiratory Syncytial Virus
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0709-2022·2022-03-09
Lacrimedics Collagen Plugs recalled for potential sterility seal compromise
Lacrimedics is recalling Collagen Plugs (models CP3, CP4, CP5) due to potential seal integrity defects in sterile pouches. The seals may contain channels that could compromise sterility and allow contamination.
Product
Collagen Plugs, CP3, 0.3mm, CP4, 0.4mm, CP5, 0.5 mm, Sterile, EO, Rx Only, CE Dry eye treatment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0714-2022·2022-03-09
Quality Control Kit Bacterial Strain Shows Unexpected Gentamicin Susceptibility
Microbiologics has recalled KWIK-STIK quality control kits due to a specific lot failing to meet resistance specifications for Gentamicin Synergy. The affected bacterial strain showed unexpected susceptibility when it should have been resistant.
Product
KWIK-STIK, Quality control kit for culture media, sold as: KWIK-STIK (single-pack) Enterococcus faecalis derived from ATCC 51299
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0704-2022·2022-03-09
Diagnostic Quality Control Material Yields False-Positive Results in GBS Testing
A quality control negative control material in GBS diagnostic testing sets is yielding false-positive results, causing laboratory test failures and operational disruptions.
Product
QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set (Live Culture). Sets include: 1. 0864E4 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 2. 0864E5 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 3. 0864E7 Streptococcus agalactiae…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0636-2022·2022-03-09
TSM Brands Isopropyl Alcohol Recalled for Undeclared Ethyl Alcohol
TSM Brands LLC is recalling Luxury 70% Isopropyl Alcohol bottles nationwide because the product contains undeclared ethyl alcohol that is not identified on the label.
Product
Luxury 70% Isopropyl Alcohol, 16 FL. OZ. (1PT) 473 ML bottle, Distributed by: TSM Brands LLC, 540 Equinox Ln, Manalapan, NJ 07726, UPC 868275965734.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0635-2022·2022-03-09
70% Isopropyl Alcohol First Aid Antiseptic Contains Undeclared Ethyl Alcohol
TSM Brands LLC is recalling 70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen due to undeclared ethyl alcohol in the product. The recall affects bottles distributed nationwide.
Product
70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen, 12 FL. OZ. 355 ML bottle, Distributed By: TSM Brands LLC, 540 Equinox LN, Manalapan, NJ 07726, www.tsmbrands.com, Made in Turkey, UPC 868275965765
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0697-2022·2022-03-09
Microbiologics QC Panel Recalled Due to Shelf Life Testing Failure
Microbiologics Inc is recalling its Helix Elite Extended Enteric Bacterial Verification Panel because real-time shelf life testing failed at 24 months.
Product
Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial Verification Panel (Inactivated Pellet) includes 21 pellets each comprised of the following 8 organisms: 1. S. Typhimurium derived from NCTC 74, 2. S. sonnei derived from NCTC 12984, 3. E. coli…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0632-2022·2022-03-09
Amlodipine and Olmesartan Medoxomil Tablets Recalled for cGMP Deviations
Macleods Pharma USA is recalling one lot of Amlodipine and Olmesartan Medoxomil Tablets nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and was initiated by the manufacturer.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0703-2022·2022-03-09
QC Control Sets for GBS Testing Recalled Due to Contamination
Microbiologics QC sets used for GBS testing contain a negative control contaminated with Group B Streptococcus, causing test failures. Affects 541 units distributed nationwide.
Product
QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set (Live Culture). Sets include: 1. 0864E3 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 2. 0864E5 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 3. 0864E7 Streptococcus agalactiae…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0642-2022·2022-03-09
Alprazolam Tablets 1mg Recalled for CGMP Deviations
Preferred Pharmaceuticals is recalling 276 bottles of Alprazolam Tablets USP 1mg (generic Xanax) distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall was initiated voluntarily by the manufacturer.
Product
Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) 30 tablets per bottle, NDC: 68788-6381-03, b) 60 tablets per bottle, NDC: 68788-6381-06, c) 90 tablets per bottle, NDC: 68788-6381-09, Mfg: Par Pharmaceutical.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0713-2022·2022-03-09
LYFO-DISK Quality Control Kit Lot Fails Antibiotic Resistance Specification
A lot of LYFO-DISK quality control kit was found susceptible to Gentamicin Synergy when it should have been resistant. The 153 affected units were distributed worldwide.
Product
LYFO-DISK, Quality control kit for culture media, sold as: LYFO-DISK Enterococcus faecalis derived from ATCC 51299
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0683-2022·2022-03-09
BioPro Titanium MPJ Toe Implant Recalled for Incorrect MR Compatibility Labeling
BioPro is recalling Titanium MPJ toe implants because instructions and patient cards falsely claim the devices are compatible with MRI imaging, when safety testing for this titanium version has not been conducted.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0639-2022·2022-03-09
Olanzapine 10 mg tablets recalled due to cGMP deviations
Macleods Pharma USA is voluntarily recalling Olanzapine 10 mg tablets nationwide due to cGMP (current good manufacturing practices) deviations identified during manufacturing. The recall affects 3,672 bottles distributed across the United States.
Product
OLANZAPINE — OLANZAPINE (OLANZAPINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0713-2022·2022-03-09
Dexamethasone Elixir Recalled for Impurities Above Permissible Levels
Morton Grove Pharmaceuticals is recalling Dexamethasone Elixir USP 0.5 mg/5 mL nationwide due to unknown impurities found at higher than permissible levels in affected lots.
Product
Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-466-08.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V136000·2022-03-08
Triple E Recalls Motorhomes Due to Missing Refrigerator Exhaust Deflectors
Triple E is recalling 2010-2014 Unity, Libero, and Serenity motorhomes because missing refrigerator exhaust deflectors allow heat to overheat the wood frame, posing a fire risk.
Product
TRIPLE E — TRIPLE E SERENITY, LIBERO, UNITY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V131000·2022-03-08
Mercedes-Benz Recalls 2021 Sprinter Vans Due to Torsion Bar Assembly Error
Daimler Vans USA is recalling 2,153 2021 Mercedes-Benz Sprinter vans because an incorrectly installed shim on the torsion bar may fail, causing loss of vehicle stability and increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 4500, SPRINTER 3500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V134000·2022-03-08
Mercedes-Benz Recalls Metris Vans Due to Fuel Hose Leak Risk
Daimler Vans USA is recalling 2017-2022 Mercedes-Benz Metris vehicles because insecure fuel hose connections may cause leaks, increasing fire risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V138000·2022-03-08
Terex Recalls 2016-2021 Aerial Devices Due to Emergency Stop Defect
Terex is recalling 2016-2021 OM, Optima-HRX, and TCX aerial devices because emergency stop controls may fail to stop all boom functions, increasing injury risk.
Product
TEREX — TEREX OPTIMA TCX, OPTIMA HRX, OM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V137000·2022-03-08
GMC Recalls 2010-2017 Terrain Vehicles for Headlight Glare Safety Issue
General Motors is recalling 2010-2017 GMC Terrain vehicles because headlight housings may reflect excessive light, causing glare for other drivers and increasing crash risk.
Product
GMC — GMC TERRAIN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V135000·2022-03-08
2022 Forest River Cardinal travel trailers recalled for electrical fire risk
Forest River is recalling certain 2022 Cardinal and related travel trailers due to a loose wire cord at the 50AMP shore power inlet that may cause an electrical short and fire.
Product
COACHMEN — COACHMEN, FOREST RIVER FREEDOM EXPRESS, CHEROKEE, SABRE, APEX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V130000·2022-03-07
Yamaha Recalls 2021-2022 MT-09 and Tracer 9 GT Motorcycles for ECU Defect
Yamaha is recalling 2021-2022 MT-09 and Tracer 9 GT motorcycles because improper ECU programming may cause engine stalls or limit throttle response, increasing crash risk.
Product
YAMAHA — YAMAHA MT-09, TRACER 9 GT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V132000·2022-03-07
Ubco Recalls 2021-2022 2X2 ADV Motorcycles Due to Wheel Hub Gear Defect
Ubco is recalling 2021-2022 2X2 ADV motorcycles because a wheel hub gear may loosen and contact the motor, potentially causing the wheel to seize and increasing crash risk.
Product
UBCO — UBCO 2X2 ADV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V125000·2022-03-04
Mercedes-Benz Recalls 2020-2021 Models for Rear Brake Caliper Fastener Issue
Mercedes-Benz is recalling 2020 AMG CLA 35 and 2021 GLA 250 vehicles because loose rear brake caliper fasteners may reduce braking performance or cause parts to detach.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLA 250, AMG CLA35
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V126000·2022-03-04
Midwest Automotive Designs Recalls 2018-2020 Sprinter Vans Due to Fire Risk
Midwest Automotive Designs is recalling 2018-2020 Passage, Weekender, and Daycruiser Sprinter Vans because a circuit board may overheat and cause a fire.
Product
MIDWEST AUTOMOTIVE DESIGN — MIDWEST AUTOMOTIVE DESIGN PASSAGE, WEEKENDER, DAYCRUISER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V124000·2022-03-04
Mercedes-Benz Recalls 2021 S 580 Vehicles for Air Bag Control Unit Defect
Mercedes-Benz is recalling 2021 S 580 4Matic vehicles because the air bag control unit may be improperly secured, risking unintentional or improper deployment.
Product
MERCEDES-BENZ — MERCEDES-BENZ S 580
Category
Vehicle
Distribution
Distributed nationwide