The Recall Desk

State

US Virgin Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44676–44700 of 73984

  • HighFDA (Devices)·Z-1051-2017·2017-01-25

    Great Basin Staph ID/R Blood Culture Panel Recalled for False Positives

    Great Basin Scientific is recalling the Staph ID/R Blood Culture Panel because the S. aureus probe could result in false positive results.

    Product
    Great Basin Staph lD/R Blood Culture Panel The Great Basin Staph lD/R Blood Culture Panel is a qualitative, multiplex in vitro diagnostic assay intended for use with the P4500 PortraitrM Analyzer System. The Staph lD/R Blood Culture Panel is capable of simultaneous detection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1264-2017·2017-01-25

    Herr Foods Recalls Chipotle Potato Chips Due to Salmonella Risk

    Herr Foods is recalling 2.0 oz. Chipotle flavored Kettle Potato Chips because the seasoning contains a milk ingredient with a potential risk of Salmonella contamination.

    Product
    Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.0 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17E006000·2017-01-25

    FRAM G2 Inline Fuel Filters Recalled for Potential Fuel Leak Risk

    UCI-FRAM is recalling FRAM Model G2 inline fuel filters because oversized connection hoses may cause fuel leaks, increasing fire risk.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1034-2017·2017-01-25

    Ultradent NanoTips 30g Dental Tips Recalled for Loose Cannula

    Ultradent Products, Inc. is recalling NanoTips 30g dental tips because the stainless steel cannula may detach from the base, posing a risk during intra-oral procedures.

    Product
    NanoTips 30g 20pk, 100pk PN 1240, 1426 Description: NanoTips are injection molded royal blue tips that contain stainless steel 30-gauge cannula to aid in the delivery of chemicals. The NanoTip base is made from a polypropylene copolymer. The stainless steel cannula is made from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1028-2017·2017-01-25

    Fresenius 2008K2 Hemodialysis System Recalled for Software Error

    Fresenius Medical Care is recalling 2008K2 hemodialysis systems because a software error may cause the machine to execute a cancelled ultrafiltration rate instead of the displayed rate.

    Product
    Fresenius 2008K2 Series : Hemodialysis System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1025-2017·2017-01-25

    Zimmer Biomet Recalls ArComXL Polyethylene Bearings Due to Labeling Mismatch

    Zimmer Biomet is recalling 19 ArComXL Polyethylene Bearings because packaging labels did not match the physical product inside, posing a risk of surgical delay.

    Product
    Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0436-2017·2017-01-25

    Town and Country Recalls Subpotent HCG Vials Due to Failed Potency

    Town and Country Compounding is recalling 101 vials of HCG because potency testing showed 74%, below the required 80-125% range.

    Product
    HCG (Chorionic Gonadotropin Lyopholized) II, 1000 unit vial, Rx only, Prepared by Town & Country, Compounding & Consultation Services, 106 Prospect St - 1st FL, Ridgewood, NJ 07459
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0435-2017·2017-01-25

    Sandoz Recalls Subpotent Donepezil Hydrochloride Tablets

    Sandoz Inc. is recalling specific lots of Donepezil Hydrochloride 10 mg tablets because they failed potency tests. The medication may not contain the full prescribed dose.

    Product
    Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1023-2017·2017-01-25

    Medacta M.U.S.T. Rods Recalled for Damaged Packaging and Sterility Issues

    Medacta USA Inc. is recalling 82 M.U.S.T. Rods due to damaged packaging and lack of sterility assurance. The recall covers units distributed in the US and several international countries.

    Product
    Medacta International SA, M.U.S.T. Rod, REF 03.50.433, Size 5.5mm, Length 480mm, Type Straight, Mat Co-Cr-Mo The rods act as a connector between the different pedicle screws to create a stable construct for the stabilization and fusion of the lumbar and thoracic spine.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1039-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Update

    Endologix is updating the Instructions for Use and implementing modifications to the AFX Endovascular AAA System.

    Product
    AFX Endovascular AAA System, Endoleak Type: IIIB Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, Endovascular Graft, Aortic Aneurysm Treatment The AFX Endovascular AAA System is intended for endovascular treatment of patients with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1049-2017·2017-01-25

    Endologix AFX2 Endovascular AAA System Recall for Updated Endoleak Information

    Endologix is recalling the AFX2 Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.

    Product
    AFX2 Endovascular AAA System Item No. Item Description F00820-01 BEA28-120/I20-40 F00820-02 BEA28-100/I20-40 F00820-03 BEA28-80/I20-40 F00820-06 BEA28-120/I16-40 F00820-07 BEA28-100/I16-40 F00820-08 BEA28-80/I16-40 F00820-09 BEA28-60/I16-40 F00820-16…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0434-2017·2017-01-25

    Perrigo Recalls Clindamycin and Benzoyl Peroxide Gel Due to Mold

    L. Perrigo Company is recalling 162,534 tubes of Clindamycin Phosphate and Benzoyl Peroxide Gel because a small number of tubes may contain mold on the cap.

    Product
    CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE — CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE (CLINDAMYCIN, BENZOYL PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1024-2017·2017-01-25

    Zimmer Biomet Recalls ArComXL Polyethylene Liners Due to Labeling Mismatch

    Zimmer Biomet is recalling 36 units of ArComXL polyethylene liners because packaging labels did not match the physical product, posing a risk of surgical delay.

    Product
    RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1037-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Updated

    Endologix updated the Instructions for Use and modified the AFX Endovascular AAA System. The correction applies to procedures conducted after July 2015.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIA Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, Endovascular Graft, Aortic Aneurysm Treatment The AFX Endovascular AAA System is intended for endovascular treatment of patients with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1048-2017·2017-01-25

    Endologix AFX Endovascular AAA System Recall for Updated Endoleak Information

    Endologix is recalling 34 units of the AFX Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.

    Product
    AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75 V F0070308 A2828/C75 V F0070312 A3434/C80 V f00553 I1616/C55F SA F00556 I2013/C70F SA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1041-2017·2017-01-25

    Smith & Nephew RENASYS GO Wound Therapy Recall for Clearance Issue

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy devices because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2017·2017-01-25

    Smith & Nephew RENASYS GO Power Supply Recalled for Regulatory Clearance

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy External Power Supply Units because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0433-2017·2017-01-25

    Novum Pharma Recalls Subpotent Novacort Gel Sample Packets

    Novum Pharma is recalling Novacort Gel sample packets because the pramoxine hydrochloride content was found to be out of specification.

    Product
    Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets), NDC 69646-704-38 (10 ct. Carton of 1gm samples) / NDC 69646-704-01 (Individual 1gm Samples within Carton), Rx Only, Novum Pharma LLC, Chicago, IL 60654
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0431-2017·2017-01-25

    Teva Recalls Risedronate Sodium Tablets for Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling 6,800 cartons of Risedronate Sodium Delayed-release Tablets, 35 mg, because they failed dissolution specifications.

    Product
    Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V052000·2017-01-24

    Ford Recalls 2016 Focus and C-Max for Floor Pan Welding Defect

    Ford is recalling 2016 Focus and C-Max vehicles because improperly welded floor pan joints may reduce structural integrity, increasing injury risk in a crash.

    Product
    FORD — FORD C-MAX, FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17071·2017-01-24

    HP Recalls Lithium-Ion Notebook Batteries Due to Fire and Burn Hazards

    HP is expanding a recall of about 101,000 lithium-ion batteries for HP and Compaq notebook computers because they can overheat, posing fire and burn risks.

    Product
    Lithium-ion batteries used in HP notebook computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V051000·2017-01-24

    Toyota Recalls 2016-2017 Tundra Trucks for Rear Bumper Defect

    Toyota is recalling 2016-2017 Tundra trucks with resin rear bumpers because the brackets may break if stepped on, posing an injury risk.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V053000·2017-01-24

    Ford Recalls 2017 F-150 Trucks Due to Instrument Cluster Power Loss

    Ford is recalling 2017 F-150 trucks because the instrument cluster may lose power in cold weather, potentially hiding the transmission gear position and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide