The Recall Desk

State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35551–35575 of 73915

  • ModerateFDA (Drugs)·D-0381-2019·2019-01-23

    Teva Recalls Olmesartan Medoxomil and Hydrochlorothiazide Tablets for Dissolution Failure

    Teva Pharmaceuticals USA is recalling specific lots of Olmesartan Medoxomil and Hydrochlorothiazide Tablets because they failed to meet dissolution specifications.

    Product
    Olmesartan Medoxomil and Hydrochlorothiazide Tablets, 40 mg/25 mg, packaged in a) 30-count bottle (NDC 0093-7617-56), b) 90-count bottle (NDC 0093-7617-98), Rx only, Manufactured In Israel By: Teva Pharmaceutical, IND. LTD., Jerusalem, 9777402, Israel, Manufactured For: Teva…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0723-2019·2019-01-23

    Arrow Pediatric Central Venous Catheter Recalled for Incorrect Labeling

    Arrow International Inc. is recalling specific lots of pediatric central venous catheters because the lidstock labels list incorrect priming volumes and flow rates.

    Product
    Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm, Reference # CS-12402 The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0371-2019·2019-01-23

    Recall of Curaplex Epi Safe Kits Due to Expired Epinephrine Vials

    Bound Tree Medical is recalling 84 Curaplex Epi Safe Administration and Training Kits because the epinephrine vials inside expired in December 2018, despite the outer label showing January 2020.

    Product
    curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit contains 2 Epi Safe Administration Kit (8600-01101) and 1 Epi Safe Training Kit (8600-01102), Rx Only. Distributed by Sarnova HC, LLC's family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0379-2019·2019-01-23

    Bound Tree Medical Recalls Curaplex Epi Safe Kits Due to Labeling Errors

    Bound Tree Medical is recalling 747 Curaplex Epi Safe Kits because they are incorrectly labeled with an expiration date of May 2018 instead of May 2019, and the syringe component lacks 510(k) clearance.

    Product
    Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe Syringe, 1 Safety needle, 2 Alcohol Prep Pads,1 Adhesive Dressing, 1 Insert. Distributed by Sarnova, HC. LLC's family companies: Bound Tree Medical. LLC, Cardio Partners, Inc., Emergency Medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V048000·2019-01-22

    Forest River Recalls 2017-2019 Motorhomes Due to Fire Risk

    Forest River is recalling 2017-2019 Glaval Entourage and Berkshire Coach Ultra motorhomes because a block heater cable defect may cause a fire.

    Product
    GLAVAL BUS — GLAVAL BUS, FOREST RIVER ENTOURAGE, BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V047000·2019-01-21

    Mack Trucks Recalls 2018 Anthem and Pinnacle Models for Clutch Defect

    Mack Trucks is recalling 2018 Anthem and Pinnacle vehicles because a clutch component may fail, causing unintended movement and increasing crash risk.

    Product
    MACK — MACK PINNACLE (CXU), ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·003-2019·2019-01-18

    Johnsonville Recalls Raw Pork Patties Due to Black Rubber Contamination

    Johnsonville is recalling raw ground pork patties potentially contaminated with black rubber. Consumers should discard or return the affected products.

    Product
    Johnsonville, LLC — Johnsonville, LLC Recalls Raw Ground Frozen Cheddar Cheese and Bacon Flavored Pork Patty Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V044000·2019-01-18

    Hino Recalls NJ8J Trucks for Missing Front Brake Dust Shields

    Hino is recalling 2007-2019 NJ8J trucks because missing front brake dust shields can cause the vehicle to pull left in wet conditions, increasing crash risk.

    Product
    HINO — HINO NJ8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V043000·2019-01-18

    Heartland Recalls 2019 Trailers Due to Incorrect Tire Certification Labels

    Heartland is recalling 2019 Prowler and Trail Runner trailers because their Federal Certification Labels may list incorrect tire size, load range, and pressure information.

    Product
    HEARTLAND — HEARTLAND TRAIL RUNNER, PROWLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V040000·2019-01-17

    Land Rover Recalls 2019 Models for Crankshaft Bolt Fracture Risk

    Jaguar Land Rover is recalling 2019 Range Rover and Discovery models because a crankshaft pulley bolt may fracture, causing engine failure and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER VELAR, RANGE ROVER, RANGE ROVER SPORT, DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2019·2019-01-17

    Perdue Recalls Gluten-Free Chicken Nuggets Due to Wood Contamination

    Perdue Foods is recalling approximately 68,244 pounds of SimplySmart Organics Gluten Free Chicken Nuggets due to possible wood contamination. Consumers should discard or return the product.

    Product
    Perdue Foods LLC — Perdue Foods LLC Recalls Simplysmart Organics Gluten Free Chicken Nugget Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V039000·2019-01-17

    Jaguar Recalls 2019 F-Pace, F-Type, and XJ for Crankshaft Bolt Defect

    Jaguar is recalling 2019 F-Pace, F-Type, and XJ vehicles because a defective crankshaft pulley bolt may fracture, causing engine failure and increasing crash risk.

    Product
    JAGUAR — JAGUAR F-PACE, F-TYPE, XJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0372-2019·2019-01-16

    Sun Pharmaceutical Recalls Vecuronium Bromide Due to Glass Particulates

    Sun Pharmaceutical Industries is recalling Vecuronium Bromide for Injection because glass particles were detected in the product.

    Product
    VECURONIUM BROMIDE — VECURONIUM BROMIDE (VECURONIUM BROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0358-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Rubber Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP due to the presence of grey rubber particulate matter in the vials.

    Product
    Ceftriaxone for Injection USP, 2 g, packaged in 10 Single Use Vials (NDC 68180-644-01) per box, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0352-2019·2019-01-16

    Heritage Pharmaceuticals Recalls Cidofovir Injection Due to Sterility Concerns

    Heritage Pharmaceuticals is recalling Cidofovir Injection vials due to complaints about dried powder on the outside of the bottles, which raises concerns about sterility.

    Product
    Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials, Rx only, Mfd by: Emcure Pharmaceuticals Ltd., Hinjawadi, Pune, India Mfg. for : Heritage Pharmaceuticals Inc. NDC 23155-0216-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0351-2019·2019-01-16

    Baxter Recalls Dianeal Low Calcium Dialysis Solution Due to Sterility Concerns

    Baxter Healthcare is recalling 29,370 bags of Dianeal Low Calcium peritoneal dialysis solution because confirmed customer complaints identified leaks in the tubing, compromising sterility.

    Product
    DIANEAL LOW CALCIUM WITH DEXTROSE — DIANEAL LOW CALCIUM WITH DEXTROSE (SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0357-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Rubber Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP vials because grey rubber flecks were found in the reconstituted product.

    Product
    Ceftriaxone for Injection USP, 1 g, packaged in a) one Single Use Vial (NDC 68180-633-01) and b) 10 Single Use Vials per box (NDC 68180-633-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0355-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Rubber Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 250 mg, due to the presence of grey rubber particulate matter from stoppers in reconstituted vials.

    Product
    Ceftriaxone for Injection USP, 250 mg, packaged in a) one Single Use Vial (NDC 68180-611-01) and b) 10 Single Use Vials per box (NDC 68180-611-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0356-2019·2019-01-16

    Lupin Recalls Ceftriaxone Injection Vials Due to Particulate Matter

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 500 mg, due to the presence of grey rubber particulate matter from stoppers.

    Product
    Ceftriaxone for Injection USP, 500 mg, packaged in a) one Single Use Vial (NDC 68180-622-01) and b) 10 Single Use Vials per box (NDC 68180-622-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V019000·2019-01-16

    GM Recalls 2010-2011 Chevrolet Malibu for Air Bag Inflator Defect

    General Motors is recalling 2010-2011 Chevrolet Malibu vehicles because the driver's air bag inflator may explode during a crash, potentially causing serious injury or death.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide