State

US Virgin Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45176–45200 of 73987

SevereFDA (Drugs)·D-0202-2017·2016-12-21
Cantrell Drug Recalls Rocuronium Bromide Syringes Due to Sterility Concerns
Cantrell Drug Company is recalling 5,067 syringes of Rocuronium Bromide 50 mg/5 mL injection solution nationwide due to a lack of assurance of sterility.
Product
Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe, Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-064-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0188-2017·2016-12-21
Cantrell Drug Recalls Fentanyl Citrate Bags Due to Sterility Concerns
Cantrell Drug Company is recalling 471 bags of Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Product
Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-35
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0191-2017·2016-12-21
Cantrell Drug Recalls Glycopyrrolate Injection Due to Sterility Concerns
Cantrell Drug Company is recalling specific lots of Glycopyrrolate injection because the firm cannot assure the sterility of the product.
Product
Glycopyrrolate 1 mg/5 mL (0.2 mg/mL) Injection Solution, 5 mL Single-Dose Syringe, For IV Use, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-028-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0192-2017·2016-12-21
Cantrell Drug Recalls Heparin Sodium Syringes Due to Sterility Concerns
Cantrell Drug Company is recalling 1,494 syringes of Heparin Sodium due to a lack of assurance of sterility. The products were distributed nationwide.
Product
Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0193-2017·2016-12-21
Cantrell Drug Recalls Heparin Sodium Bags Due to Sterility Concerns
Cantrell Drug Company is recalling 150 bags of Heparin Sodium 5,000 USP Units in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Product
Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/Office Use Only, Injection Solution For IV Use, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-097-24
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V922000·2016-12-21
GM Recalls 2016 Buick Envision for Brake Line Cracking Risk
General Motors is recalling 2016 Buick Envision vehicles because master cylinder brake lines may crack and leak fluid, potentially reducing braking performance.
Product
BUICK — BUICK ENVISION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V919000·2016-12-21
BMW Recalls 2016 X5 xDrive40e Vehicles Due to Electrical Ground Cable Issue
BMW is recalling 2016 X5 xDrive40e vehicles because a loose electrical ground cable may cause the transmission to shift to neutral, increasing crash risk.
Product
BMW — BMW X5
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0190-2017·2016-12-21
Cantrell Drug Company Recalls Fentanyl and Bupivacaine Bags for Sterility Concerns
Cantrell Drug Company is recalling specific lots of Fentanyl Citrate and Bupivacaine HCl bags due to a lack of assurance of sterility.
Product
Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride, 100 mL* Bag, Epidural Use Only, Single-Dose Bag, Hospital/Office Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-080-75
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0198-2017·2016-12-21
Cantrell Drug Recalls Midazolam HCl Syringes Due to Sterility Concerns
Cantrell Drug Company is recalling 37 syringes of Midazolam HCl 50 mg/50 mL due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Midazolam HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL), Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-001-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0187-2017·2016-12-21
Cantrell Drug Recalls Calcium Chloride Injection Due to Sterility Concerns
Cantrell Drug Company is recalling 645 vials of Calcium Chloride Injection Solution because the firm cannot assure the sterility of the product.
Product
Calcium Chloride, (1 g/10 mL) Injection Solution 10 mL, 10% Single-Dose Vial, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0199-2017·2016-12-21
Cantrell Drug Recalls Morphine Sulfate Bags Due to Sterility Concerns
Cantrell Drug Company is recalling 1,748 bags of Morphine Sulfate 1 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride, 100 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-160-75
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0195-2017·2016-12-21
Cantrell Drug Recalls Hydromorphone Syringes Due to Sterility Concerns
Cantrell Drug Company is recalling 935 vials of Hydromorphone HCl 50 mg/50 mL single-dose syringes due to a lack of assurance of sterility.
Product
HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0184-2017·2016-12-21
Cantrell Drug Recalls Calcium Chloride Bags Due to Sterility Concerns
Cantrell Drug Company is recalling 80 bags of Calcium Chloride 1 g/50 mL due to a lack of assurance of sterility.
Product
Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)*, Single-Dose Bag, Rx Only, Hospital/Office Use Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-175-37
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0185-2017·2016-12-21
Cantrell Drug Company Recalls Phenylephrine HCl Syringes Due to Sterility Concerns
Cantrell Drug Company is recalling 30,796 syringes of Phenylephrine HCl 1 mg/10 mL due to a lack of assurance of sterility. The recall covers products distributed nationwide.
Product
Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-171-12
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0200-2017·2016-12-21
Cantrell Drug Recalls Neostigmine Methylsulfate Syringes Due to Sterility Concerns
Cantrell Drug Company is recalling specific lots of Neostigmine Methylsulfate injection syringes because the firm cannot ensure the products are sterile.
Product
Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose Syringe, For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-046-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0201-2017·2016-12-21
Cantrell Drug Company Recalls Oxytocin Injection Bags Due to Sterility Concerns
Cantrell Drug Company is recalling 2,681 bags of Oxytocin 30 USP Units due to a lack of assurance of sterility. The affected product is distributed nationwide.
Product
Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag, Single-Dose Bag, Injection Solution for IV Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-056-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0197-2017·2016-12-21
Cantrell Drug Recalls Lidocaine HCl Syringes Due to Sterility Concerns
Cantrell Drug Company is recalling 162 syringes of Lidocaine HCl 1% because the firm cannot assure the sterility of the product.
Product
Lidocaine HCl 1%, 10 mL Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0196-2017·2016-12-21
Cantrell Drug Recalls Hydromorphone Injection Vials Due to Sterility Concerns
Cantrell Drug Company is recalling 93 vials of Hydromorphone HCl injection solution nationwide due to a lack of assurance of sterility.
Product
Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial (1 mg/mL), Single-Dose Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0186-2017·2016-12-21
Cantrell Drug Company Recalls Calcium Chloride Bags Due to Sterility Concerns
Cantrell Drug Company is recalling 73 bags of Calcium Chloride in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Product
Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0204-2017·2016-12-21
Cantrell Recalls Succinylcholine Chloride Injection Due to Sterility Concerns
Cantrell Drug Company is recalling specific lots of Succinylcholine Chloride 200 mg/10 mL injection syringes because the firm cannot ensure the products are sterile.
Product
Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-067-12
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0203-2017·2016-12-21
Cantrell Drug Recalls Ropivacaine HCl Bags Due to Sterility Concerns
Cantrell Drug Company is recalling 87 bags of Ropivacaine HCl 0.25% due to a lack of assurance of sterility. The product is intended for epidural use only.
Product
Ropivacaine HCl 0.25% in 0.9% Sodium Chloride, 100 mL Bag, Epidural Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-185-75
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0745-2017·2016-12-21
BD Vacutainer Push Button Blood Collection Set Recall for Barrel Separation
Becton Dickinson is recalling specific lots of BD Vacutainer Push Button Blood Collection Sets because the front and rear barrels may separate when the safety feature is activated.
Product
BD 23 G x .75 in. BD Vacutainer¿ Push Button Blood Collection Set with 12 in. Tubing Catalog # 367342 Intended for venipuncture to obtain blood specimens from patients.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0760-2017·2016-12-21
Inovo Purefill Oxygen Compressor Recalled for Operational Failure Risk
Inovo, Inc. is recalling 117 Inovo Purefill Oxygen Compressor Model PF1100 units because the device can fail during operation.
Product
INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen refill machine that you can attach to an oxygen concentrator to refill portable oxygen cylinders.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0746-2017·2016-12-21
Steris Recalls Harmony Insight Diagnostic Monitor Support Systems
Steris Corporation is recalling 63 Harmony Insight Diagnostic Monitor Support Systems because spring arm screws may not be properly secured and could become loose.
Product
Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm (EMS) The system is intended for use in surgical operating rooms (OR) or intraoperative surgical/imaging rooms where simultaneous multiple image viewing is required
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0765-2017·2016-12-21
Stryker Recalls Reprocessed Xcel Bladeless Trocars Due to Plug Breakage
Stryker is recalling 40,476 reprocessed Xcel Bladeless Trocars because the adjustable plug may break in packaging or during use.
Product
Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry for endoscopic instruments in patients requiring minimally invasive surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide