State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59926–59950 of 74011

HighFDA (Devices)·Z-0599-2014·2014-01-08
Asante Conset Infusion Set Recalled for Tubing Disconnection and Insulin Leakage
Asante Solutions is recalling Conset Infusion Sets because the tubing may disconnect from the connector, causing insulin leakage and delivering less insulin than intended.
Product
Asante Conset Infusion Set with 60cm tubing & 9mm cannula packaged in 5-packs,singles, or inside a Combination Kit (FG-5229-4); Distributed by Asante Solutions, Sunnyvale, CA; Manufactured by Convatec; Lejre, Denmark.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0618-2014·2014-01-08
Stryker S3 Med/Surg Bed Recall for Foot End Cover Damage
Stryker is recalling S3 Med/Surg beds due to potential damage to the Foot End Cover and Power Coil Cable caused by reduced clearance.
Product
S3 Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals. The bed is designed for a 15 year expected service life under normal use conditions, and with appropriate periodic maintenance as described in the maintenance manual…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0605-2014·2014-01-08
Steris Recalls Verify Dual Species Biological Indicators Due to Spore Count Defect
Steris is recalling Verify Dual Species Self-Contained Biological Indicators because the spore count is lower than labeled, potentially causing false sterilization results.
Product
VERIFY¿ Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor, OH. Intended for use in installation testing and routine monitoring of steam sterilization and ethylene oxide sterilization processes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0616-2014·2014-01-08
Steris SYSTEM 1E Liquid Chemical Sterilant Processing System Recalled for Valve Issues
Steris Corporation is recalling SYSTEM 1E Liquid Chemical Sterilant Processing Systems because check valve o-rings degrade, causing nuisance aborts.
Product
SYSTEM 1E Liquid Chemical Sterilant Processing System, Distributed by STERIS Corporation, Mentor, OH The SYSTEM 1E Liquid Chemical Sterilant Processing System is intended for the liquid chemical sterilization of manually cleaned immersible and reusable critical and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0816-2014·2014-01-08
XYMOGEN Recalls LipiChol 540 Medical Food Due to Mislabeling
Atlantic Pro Nutrients is recalling LipiChol 540 because it was labeled as a medical food instead of a dietary supplement.
Product
LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription Distributed by: PharmaceutiX Orlando, Florida
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-396-2014·2014-01-08
Teva Recalls Niacin Extended Release Tablets Due to Broken Tablets
Teva Pharmaceuticals is recalling Niacin Extended Release Tablets, 500 mg, because the tablets may be broken.
Product
Niacin Extended Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., Sellersville, PA, 18960, NDC 0093-7392-98
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0615-2014·2014-01-08
Synthes Electric Pen Drive Hand Switch Recalled for Labeling Error
Synthes USA HQ, Inc. is recalling 290 Electric Pen Drive Hand Switches because the 'on' and 'lock' labels were interchanged.
Product
Synthes Hand Switch - Electric Pen Drive, Part Number 05.001.012 The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and metal, drilling, decorticating, shaping, and smoothing of bones and teeth in a wide variety of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0606-2014·2014-01-08
RTC 25-C Inline Aerosol Tee Adapter Recalled for Incomplete Instructions
Instrumentation Industries Inc. is recalling 220 units of the RTC 25-C Inline Aerosol Tee Adapter because some packages were shipped with incomplete installation and usage directions due to a printing error.
Product
RTC 25-C Inline Aerosol Tee Adapter. Intended to be used to adapt an aerosolized medication delivery system having an elliptical mouthpiece to a ventilator circuit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-393-2014·2014-01-08
Sandoz Recalls Subpotent Fosinopril Sodium and Hydrochlorothiazide Tablets
Sandoz Inc. is recalling specific lots of Fosinopril Sodium and Hydrochlorothiazide tablets because the hydrochlorothiazide content was subpotent at the 9-month time point.
Product
Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC 0185-0341-01,
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-394-2014·2014-01-08
Qualitest Recalls Cetirizine Hydrochloride Syrup Due to Impurity Failure
Qualitest Pharmaceuticals is recalling 438,055 bottles of Cetirizine Hydrochloride Syrup because the product failed impurity specifications for 4-chlorobenzophenone.
Product
Cetirizine Hydrochloride Syrup (Cetirizine Hydrochloride Oral Solution, USP) 1 mg/mL, 120 mL and 480 mL bottles, Rx only. Mfg. for: Qualitest Pharmaceuticals, Huntsville, AL 35811. NDC 0603-9063-54 (120 mL), NDC 0603-9063-58 (480 mL).
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-391-2014·2014-01-08
G & W Fluocinolone Acetonide Cream Recalled for Content Uniformity Failure
G & W Laboratories is recalling Fluocinolone Acetonide Cream 0.025% because it failed content uniformity specifications at the 18-month time point.
Product
FLUOCINOLONE ACETONIDE — FLUOCINOLONE ACETONIDE (FLUOCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0614-2014·2014-01-08
Merit Medical Systems Recalls Maestro Microcatheters Due to Label Graphic Discrepancy
Merit Medical Systems is recalling 59 Maestro Microcatheters because the graphic on the carton's end panel does not match the front panel.
Product
Catheter, Continuous Flush The Merit Microcatheter is intended for general intravascular use, including peripheral and coronary vasculature. Once the subselective region has been accessed, the microcatheter can be used for the controlled and selective infusion of diagnostic…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Food)·F-0815-2014·2014-01-08
XYMOGEN LipiChol Medical Food Recalled for Incorrect Product Classification
Atlantic Pro Nutrients is recalling 25,852 bottles of LipiChol and related brands because the product was labeled as a medical food instead of a dietary supplement.
Product
XYMOGEN LipiChol (Omega-3 Phospholipid 540 mg) Medical Food Distributed by Xymogen Orlando, Florida. Also sold and distributed under various brands and firms: *1. 4XLipidComplete (Omega-3 Phospholipid 540 mg) Medical Food Distributed by: N2 Health, La Quinta, CA. *2. AL…
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·14E001000·2014-01-06
Ford Recalls 2011-2012 Explorers for Steering Gear Locking Risk
Ford is recalling certain 2011-2012 Explorers because replacement steering gears may lock, preventing steering and increasing crash risk.
Product
FORD — FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V002000·2014-01-06
Ford Recalls 2012-2013 Edge Vehicles for Fuel Line Leak Risk
Ford is recalling 2012-2013 Edge vehicles with 2.0L engines because a cracked fuel line pulse damper housing may cause a fuel leak and potential fire.
Product
FORD — FORD EDGE
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·14075·2014-01-02
Walmart Recalls Mainstays Card Table and Chair Sets Due to Injury Hazards
Walmart is recalling Mainstays five-piece card table and chair sets because the chairs can collapse, posing fall and finger injury risks.
Product
Mainstays five-piece card table and chair sets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·14V001000·2014-01-02
Altec AH75, AH85, and AH100 Vehicles Recalled for Control Module Defect
Altec is recalling 2010-2013 AH75, AH85, and AH100 vehicles because moisture in the control module plug may cause the boom or platform to move unexpectedly.
Product
ALTEC — ALTEC AH75, AH85, AH100
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·14706·2014-01-02
Norwood Furniture Recalls Science Tables Due to Leg Splitting Hazard
Norwood Furniture is recalling science tables because wooden legs can split, causing instability. No injuries have been reported.
Product
Norwood Furniture Science Tables
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-1254-2014·2014-01-01
Aunt Jemima and Quaker Corn Meal Recalled for Aflatoxin Levels
Quaker Foods and Snacks North America is recalling specific Aunt Jemima and Quaker corn meal products because they contain levels of aflatoxin above the legal limit.
Product
White Corn Meal sold under the Aunt Jemima brand and packaged in a paper bag with a net weight of 80 oz. (5 lb.) 2.26 kg.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1252-2014·2014-01-01
Aunt Jemima Self-Rising Cornmeal Mix Recalled for Aflatoxin Levels
Quaker Foods and Snacks North America is recalling Aunt Jemima Self-Rising White Cornmeal Mix because it contains aflatoxin levels above the legal limit.
Product
Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand and packaged in a paper bag with a net weight respectively of 32 oz. (2 lb.) 907 g. or 5 lb. (2.26 kg.).
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1137-2014·2014-01-01
FoodState Recalls MegaZymes Plus Due to Chloramphenicol Contamination Risk
FoodState is recalling KARIKAS ORTHOMOLECULAR NUTRITION MegaZymes Plus due to potential chloramphenicol contamination. Consumers should stop using the product.
Product
KARIKAS ORTHOMOLECULAR NUTRITION MegaZymes Plus (High Concentration) (LK10528)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-388-2014·2014-01-01
GlaxoSmithKline Recalls Sumatriptan Injection Cartridges Due to Sterility Concerns
GlaxoSmithKline is recalling 9,743 cartridges of Sumatriptan Succinate Injection because some may have needles protruding through the shield, compromising sterility.
Product
Sumatriptan Succinate Injection, 6 mg, 0.5 mL For subcutaneous injection only, Rx only, 2 Single-Dose Syringe Cartridges for use with sumatriptan Autoinjector Pen, Manufactured by GlaxoSmithKline, Research Triangle Park, NC 27709 for Sandoz Inc., Princeton, NJ 08540, Made in…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1253-2014·2014-01-01
Aflatoxin Levels in Quaker and Aunt Jemima Corn Products Exceed Legal Limits
Quaker Foods and Snacks North America is recalling specific corn meal and grits products because they contain aflatoxin levels above the legal limit.
Product
White quick grits and grits packaged in a paper bag sold under the Aunt Jemima or Quaker brand and packaged in a paper bag with a net weight respectively of 36.8 oz. (2 lb. 4 oz.) 1.04 kg., 5 lb. (80 oz.) 2.26 kg., or a club pack of three 5 lb. bags bundled together.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0534-2014·2014-01-01
CareFusion Recalls Alaris PC Units Due to System Error Messages
CareFusion is recalling Alaris PC units because they may produce audible alarms and display System Error messages.
Product
Alaris PC unit model 8000 and 8015 with Alaris PCA module model 8120 and Auto ID barcode scanner model 8600. Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System. The Alaris PCA (Patient Controlled…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-387-2014·2014-01-01
FDA Recalls Imitrex STATdose Systems Due to Sterility Concerns
GlaxoSmithKline is recalling 10,469 Imitrex STATdose Systems because some syringes may have needles protruding through the shield, compromising sterility.
Product
IMITREX — IMITREX (SUMATRIPTAN)
Category
Drug
Distribution
Distributed nationwide