State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41901–41925 of 73919

SevereFDA (Drugs)·D-1022-2017·2017-08-02
SCA Pharmaceuticals Recalls Repinephrine Bitartrate Due to Sterility Concerns
SCA Pharmaceuticals is recalling Repinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL due to a lack of assurance of sterility and potential for product leakage.
Product
NORepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0775-40
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V486000·2017-08-02
CSI Recalls 2013-2016 Wildland Units Due to Wheel Cracking
CSI Emergency Apparatus is recalling 2013-2016 Wildland Emergency vehicles because Stazworks wheels may crack and break, potentially causing a crash.
Product
CSI — CSI WILDLAND UNIT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1027-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling Phenylephrine 40 mg in 0.9% Sodium Chloride 250 mL due to lack of assurance of sterility and potential for leaking.
Product
PHENYLephrine 40 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0812-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1010-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling fentanyl citrate syringes due to a lack of assurance of sterility and potential for leaking.
Product
fentaNYL as citrate 5 mcg/mL in 0.9% Sodium Chloride 1 mL in Single Dose syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0225-24
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1006-2017·2017-08-02
SCA Pharmaceuticals Recalls Bupivacaine HCl Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Bupivacaine HCl 0.125% bags due to a lack of assurance of sterility and potential for leaking.
Product
BUPIVacaine HCl 0.125% In 250 mL 0.9% Sodium Chloride Bag, Preservative Free (Total Dose Bupivacaine 312.5 mg per 250 mL), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0062-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1030-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine IV Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling Phenylephrine 20 mg IV bags due to a lack of assurance of sterility and potential for leaking.
Product
PHENYLephrine 20 mg in 0.9% Sodium Chloride 250 mL Bag, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0816-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1023-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine HCl Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine HCl injection because the product lacks assurance of sterility and has the potential to leak.
Product
PHENYLephrine HCl 60 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0809-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1033-2017·2017-08-02
SCA Pharmaceuticals Recalls Potassium Chloride Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL due to lack of assurance of sterility and potential for leaking.
Product
Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0833-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1015-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl and Bupivacaine Infusion Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of fentanyl and bupivacaine infusion bags because they may leak and lack assurance of sterility.
Product
fentaNYL 2 mcg/mL + BUPIvacaine 0.125% PF in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0254-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1019-2017·2017-08-02
SCA Pharmaceuticals Recalls Epinephrine HCl Due to Sterility Concerns
SCA Pharmaceuticals is recalling Epinephrine HCl 4 mg in 0.9% Sodium Chloride 250 mL due to a lack of assurance of sterility and potential for leaking.
Product
EPINEPHrine HCl 4 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0613-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1000-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl Citrate Injection Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 130 bags of fentanyl citrate injection due to a lack of assurance of sterility caused by potential leaks in the sodium chloride bags used.
Product
fentaNYL (as citrate) 10 mcg per mL in 0.9% Sodium Chloride, (Total fentaNYL Dose 1,000 mcg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0202-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1017-2017·2017-08-02
SCA Pharmaceuticals Recalls Hydromorphone Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Hydromorphone injection syringes because they may leak and lack assurance of sterility.
Product
Hydromorphone 0.5 mg/mL in 0.9% Sodium Chloride 1 mL Fill in 3 mL BD syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0302-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1005-2017·2017-08-02
SCA Pharmaceuticals Recalls Bupivacaine HCl Due to Sterility Concerns
SCA Pharmaceuticals is recalling Bupivacaine HCl 0.1% bags due to a lack of assurance of sterility and potential for leaking.
Product
BUPIVacaine HCl 0.1% PF (From 0.75%) in 0.9% Sodium Chloride, 250 mL Bag, Preservative Free (Waste From 250 mL Bag), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0060-40
Category
Drug
Distribution
Distributed nationwide
HighCPSC·17197·2017-08-02
Sweet Bamboo Recalls Children's Pajamas for Flammability Violation
Sweet Bamboo is recalling about 500 children's woven pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Product
Children's two-piece woven pajama sets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V485000·2017-08-02
2017 Jeep Renegade Recall for Instrument Panel Software Defect
Chrysler is recalling 2017 Jeep Renegade vehicles because a software issue may cause malfunction indicator lamps to illuminate incorrectly, potentially masking true vehicle faults.
Product
JEEP — JEEP RENEGADE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2778-2017·2017-08-02
Invuity PhotonBlade Recalled for Potential Unintended Energy Discharge
Invuity, Inc. is recalling 1,328 units of the INVUITY PhotonBlade device due to reports of unintended energy discharge that could cause tissue damage.
Product
INVUITY(R) PhotonBlade(TM), REF PB1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2886-2017·2017-08-02
Peanut Butter Spread Recalled for Missing Coconut Allergen Labeling
Peanut Butter Holdings LLC is recalling PB Crave Coconut Milk Chocolate Peanut Butter Spread because the allergen statement fails to list coconut.
Product
PB Crave, Coconut Milk Chocolate Peanut Butter Spread, NET WT 16 OZ (1 LB) -454 g. Plastic jars, 6 per case.
Category
Food
Distribution
Distributed nationwide
HighNHTSA·17E043000·2017-08-02
VMAC Underhood Air Compressors Recalled for Detaching Fan Assembly Risk
VMAC is recalling VR 150 and VR 70 Underhood Air Compressors for 2017 Ford trucks because a loose fan assembly may cause impact damage and injury.
Product
ENGINE AND ENGINE COOLING:COOLING SYSTEM:FAN recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17198·2017-08-02
Fred's Recalls Mini Barrel Charcoal Grills Due to Fire Hazard
Fred's is recalling Living Traditions mini barrel charcoal grills because the exterior paint can ignite, posing a fire hazard.
Product
Mini barrel charcoal grills
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2764-2017·2017-08-02
Medtronic Recalls DLP Extension Line Adapters Due to Packaging Pinholes
Medtronic Perfusion Systems is recalling DLP Extension Line Adapters because small pinholes were found in a single packaging configuration of sterile pouches.
Product
DLP Extension Line Adapters 20 in length Used to extend cardioplegia line during cardiopulmonary bypass surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2762-2017·2017-08-02
Fisher Diagnostics Recalls FDP Assay Kits Due to False Negative Risk
Fisher Diagnostics is recalling Pacific Hemostasis FDP Assay Kits and Latex Reagents because reduced sensitivity may cause false negative results at low FDP levels.
Product
Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI 00845275000863, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company LLC ,a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA --- For…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V484000·2017-08-02
Forest River Recalls 2018 Salem and Wildwood Trailers for Incorrect Weight Labels
Forest River is recalling 2018 Salem and Wildwood recreational trailers because the Federal Placards may state an incorrect weight, which could affect vehicle handling and increase crash risk.
Product
FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0999-2017·2017-08-02
SCA Pharmaceuticals Recalls Morphine Sulfate Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 220 bags of morphine sulfate in 0.9% sodium chloride because the product was made with recalled saline bags that may leak, compromising sterility.
Product
morphine sulfate 1 mg per mL in 0.9% Sodium Chloride, (Total morphine Dose 100 mg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, (877) 550-5059; labeled as a) NDC: 70004-0100-59; b) NDC: 70004-100-58.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2763-2017·2017-08-02
Fisher Diagnostics Recalls FDP Latex Reagent Due to Reduced Sensitivity
Fisher Diagnostics is recalling specific lots of Pacific Hemostasis FDP Latex Reagent because reduced sensitivity may cause false negative test results.
Product
Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company, LLC, a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2767-2017·2017-08-02
Medtronic Recalls DLP Pressure Monitoring Extension Line Adapters
Medtronic Perfusion Systems is recalling DLP Pressure Monitoring Extension Line Adapters due to small pinholes in sterile packaging.
Product
DLP Pressure Monitoring Extension Line Adapters Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.
Category
Medical Device
Distribution
Distributed nationwide