State

US Virgin Islands product recalls

72,986 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: 30
Most recent: 2026-09-09

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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8551–8575 of 73163

SevereFDA (Devices)·Z-0482-2025·2024-11-27
Medical Device Recall: Counterfeit Batteries in Plum Infusion Systems
Counterfeit CSB batteries are being used in Plum Infusion Systems. These unauthorized batteries fail to hold their charge and have not been tested for use with the pumps.
Product
Allegedly counterfeit batteries manufactured by CSB batteries being used with Plum Infusion Systems: Plum 360" Infusion System, Pump List Number 30010; Plum A+ & Plum A+3" Infusion Systems, Pump List Numbers: 11005, 11971, 12391, 12618, 20678, 20679, 20792, 60529, 12348, 1197
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0469-2025·2024-11-27
Posi-Stop 23-Gauge Injection Needles recalled for manufacturing debris blockage
Hobbs Medical recalls Posi-Stop Injection Needles because manufacturing debris in the needle can block injection solution flow.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0480-2025·2024-11-27
CAIRE FreeStyle Comfort Portable Oxygen Concentrator Battery Recharge Failure
Six CAIRE FreeStyle Comfort oxygen concentrators may fail to recharge their batteries, potentially affecting portable use of these medical devices. Caire, Inc. is recalling affected units worldwide.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-103.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24C002000·2024-11-27
Nuna Rava Child Seat Recall for Harness Adjuster Defect
Nuna is recalling Rava child seats where debris may cause the harness adjuster to fail, potentially leaving the harness loose in a crash.
Product
CHILD SEAT:HARNESS:FRONT ADJUSTER BUTTON/RELEASE MECHANISM recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0470-2025·2024-11-27
Posi-Stop Injection Needle Recall Due to Manufacturing Debris
Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Catalog 4706) due to manufacturing debris in the inner sheath that can block the needle and prevent injection solution flow.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0050-2025·2024-11-27
Guaifenesin Dextromethorphan Syrup Recalled for Failed Quality Specifications
Major Pharmaceuticals has recalled Guaifenesin Dextromethorphan Syrup due to failed impurity and degradation specifications. Three lot numbers were distributed nationwide.
Product
Guaifenesin Dextromethorphan Syrup, 100 mg/10mg per 5 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7134-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0380-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0381-2025·2024-11-27
Baxter MiniCap PD Transfer Set Recalled for Potential Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0049-2025·2024-11-27
Guaifenesin-Dextromethorphan Cough Syrup Recalled for Failed Impurity Specifications
Major Pharmaceuticals is recalling Guaifenesin Dextromethorphan Syrup nationwide for specific lots that failed to meet impurity and degradation specifications. Consumers should contact their pharmacist if they possess affected lots.
Product
Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2025·2024-11-27
Ramipril Capsule Medication Recalled Over Unapproved Vendor Manufacturing Deviations
Lupin Pharmaceuticals is recalling 357,414 bottles of Ramipril 10 mg capsules due to CGMP deviations where the active pharmaceutical ingredient was sourced from an unapproved vendor. The affected product was distributed to 30 wholesalers with potential nationwide distribution.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0051-2025·2024-11-27
Bevacizumab injection syringes recalled for lack of sterility assurance
27,560 bevacizumab injection syringes distributed nationwide are being recalled due to failure to maintain sterility assurance. The affected syringes may not be sterile.
Product
BEVACIZUMAB (AVASTIN)1.25mg/0.05mL, Sterile Injection, 0.5 mL Single-Dose Syringe, Rx Only, Repackaged by: Medivant Healthcare: 24416 N 19th Ave, Phoenix, AZ, NDC 81483-0041-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0055-2025·2024-11-27
Prescription Dextroamphetamine Patches Recalled for Defective Adhesive System
Noven Pharmaceuticals Inc is recalling 685 boxes of XELSTRYM (dextroamphetamine) transdermal patches nationwide due to a defect in the adhesive delivery system. The product does not meet manufacturing specifications.
Product
XELSTRYM — XELSTRYM (DEXTROAMPHETAMINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0060-2025·2024-11-27
Docusate Sodium 250 mg softgels recalled due to defective blister packaging
Safecor Health is recalling Docusate Sodium 250 mg softgels due to manufacturing defects where blister card-foils separated from the medication cavity, potentially compromising product integrity.
Product
Docusate Sodium 250 mg, 1 Softgel in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-101-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls found in similar devices.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0140-2025·2024-11-27
Great Value Cheese Danish Recalled for Plastic Pieces
Great Value Cheese Danish is being recalled due to plastic pieces found in the product. Consumers who purchased this item should discard it.
Product
Great Value Cheese Danish 16.5 oz UPC 078742201177, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0473-2025·2024-11-27
Posi-Stop Injection Needles recalled for manufacturing debris blockage
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris that can block needle flow. Some units may contain debris in the inner sheath that prevents injection solutions from functioning properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2025·2024-11-27
JuggerLoc/ToggleLoc 2.9mm Drill Guide Warping in Packaging
Biomet's JuggerLoc/ToggleLoc 2.9mm Drill Guide may warp when removed from packaging, potentially extending surgical time or causing tissue damage requiring intervention.
Product
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2025·2024-11-27
CAIRE FreeStyle Comfort portable oxygen concentrator battery recharge failure
Caire Inc. is recalling 26 CAIRE FreeStyle Comfort portable oxygen concentrators due to potential battery recharge failure. Affected units identified by serial number may not charge properly.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2025·2024-11-27
Posi-Stop 25-Gauge Injection Needles Recalled for Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop 25-Gauge injection needles because some units contain manufacturing debris that blocks the needle's inner diameter, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0485-2025·2024-11-27
Acrobat SUV Vacuum Stabilizer System Sterile Barrier Compromise Recall
Maquet Cardiovascular is recalling the Acrobat SUV Vacuum Stabilizer System (Model C-OM-9000Z) due to manufacturing deviations that compromise the sterile barrier. Sterility cannot be assured during the 2-year shelf life, affecting approximately 10,778 units.
Product
Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000Z
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0486-2025·2024-11-27
Acrobat-i Vacuum Stabilizer System Recalled for Sterile Barrier Compromise
Maquet Cardiovascular is recalling approximately 33,823 units of the Acrobat-i Vacuum Stabilizer System due to manufacturing deviations that compromised the sterile barrier. Sterility cannot be assured for the 2-year shelf life.
Product
Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V895000·2024-11-27
Forest River Recalls 2025 Motorhomes Due to Taillight Overheating and Failure
Forest River is recalling 2025 Concord, Entourage, Freelander, and Leprechaun motorhomes because taillights may overheat and fail to illuminate, increasing crash risk.
Product
FOREST RIVER — FOREST RIVER FREELANDER, CONCORD, LEPRECHAUN, ENTOURAGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V898000·2024-11-27
Audi plug-in hybrid high voltage batteries can overheat
Volkswagen is recalling certain 2022-2023 Audi Q5 PHEV and 2022 Audi A7 PHEV vehicles because the high-voltage battery may overheat, increasing the risk of a fire.
Product
AUDI — AUDI Q5, A7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0484-2025·2024-11-27
Maquet Cardiovascular Recalls Acrobat-i Positioners Due to Sterility Concerns
Maquet Cardiovascular is recalling 14,338 Acrobat-i Positioners because manufacturing deviations compromised the sterile barrier, meaning sterility cannot be assured during the product's 2-year shelf life.
Product
Acrobat-i Positioner. Model Number C-XP-5000Z
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0061-2025·2024-11-27
Lisinopril 10 mg Tablets Recalled for Metal Fragment Contamination
Evaric Pharmaceuticals is recalling Lisinopril 10 mg tablets after a metal fragment was found embedded in a tablet. The affected lot (241103) was distributed nationwide; contact your pharmacist if you have this medication.
Product
LISINOPRIL — LISINOPRIL (LISINOPRIL)
Category
Drug
Distribution
Distributed nationwide