The Recall Desk

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.

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.

45251–45275 of 73987

  • HighNHTSA·16V903000·2016-12-15

    Mercedes-Benz Recalls SUVs for Front Passenger Air Bag Defect

    Mercedes-Benz is recalling specific 2016-2017 SUVs because the front passenger air bag may not deploy due to a calibration error.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE350, GLE400, AMG GLE43, AMG GLE63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0634-2017·2016-12-14

    Cento Romano Grated Cheese Recalled Due to Salmonella Contamination

    4 C Foods, Corp. is recalling Cento Romano Grated Cheese because FDA samples revealed Salmonella contamination. Consumers should stop using the product.

    Product
    Cento Romano Grated Cheese, UPC 70796-90501, 6 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0631-2017·2016-12-14

    4C Homestyle Grated Cheese Recalled for Salmonella Contamination

    4 C Foods, Corp. is recalling 4C Homestyle All Natural Parmesan/Romano Grated Cheese because FDA samples revealed Salmonella contamination.

    Product
    4C Homestyle All Natural Parmesan/Romano Grated Cheese, UPC 41387-11627, 6 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0630-2017·2016-12-14

    4C Homestyle Parmesan Grated Cheese Recalled for Salmonella Contamination

    4 C Foods, Corp. is recalling 4C Homestyle All Natural Parmesan Grated Cheese because FDA samples revealed Salmonella contamination.

    Product
    4C Homestyle All Natural Parmesan Grated Cheese, UPC 41387-32790, 6 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0632-2017·2016-12-14

    4C Homestyle Pecorino Romano Cheese Recalled for Salmonella Contamination

    4 C Foods, Corp. is recalling 4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese because FDA samples revealed Salmonella contamination.

    Product
    4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese, UPC 41387-12302, 6 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0177-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Range Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.

    Product
    Range Trauma Kit - Product Code 85-1274, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0629-2017·2016-12-14

    4C Pecorino Romano Cheese Recalled Due to Salmonella Contamination

    4 C Foods, Corp. is recalling 4C All Natural 100% Imported Italian Pecorino Romano Cheese because FDA samples revealed Salmonella contamination.

    Product
    4C All Natural 100% Imported Italian Pecorino Romano Cheese, UPC 41387-77126, 6 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0625-2017·2016-12-14

    Kraft Heinz Recalls Weight Watchers Chocolate Chip Cookie Dough Sundaes

    Kraft Heinz is recalling Weight Watchers Smart Ones Chocolate Chip Cookie Dough Sundaes due to possible Listeria monocytogenes contamination.

    Product
    Weight Watchers Smart Ones, Chocolate Chip Cookie Dough Sundae, Keep Frozen, 4 Individual Sundaes, 4-2.11 OZ (60g), NET WT. 8.44 OZ (239g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0633-2017·2016-12-14

    Cento Parmesan Grated Cheese Recalled for Salmonella Contamination

    4 C Foods, Corp. is recalling Cento Parmesan Grated Cheese because FDA samples revealed Salmonella contamination. Consumers should stop using the product.

    Product
    Cento Parmesan Grated Cheese, UPC 70796-90502, 6 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0181-2017·2016-12-14

    North American Rescue Recalls Mini Resupply Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Mini Resupply Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.

    Product
    Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0647-2017·2016-12-14

    Centurion Multi-Med Single Lumen Catheters Recalled for Embolism Risk

    Centurion Medical Products is recalling 1,000 Multi-Med Single Lumen Catheter kits because excess material at the catheter tip may separate and cause an embolism.

    Product
    Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in patients requiring administration of solutions, blood sampling, and central venous pressure monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0178-2017·2016-12-14

    North American Rescue Recalls Advance Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Advance Trauma Kits because the manufacturer has concerns regarding the sterility of the eye wash irrigating solution.

    Product
    Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0702-2017·2016-12-14

    Thayer MANOS EX Surgical Device Recalled for Missing Safety Warning

    Thayer Intellectual Property, Inc. is recalling 339 MANOS EX surgical devices because customers were not notified of a critical safety warning regarding device bending and breakage.

    Product
    MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal ligament in patients with Carpal Tunnel Syndrome who fail conservative therapy. Plantar Fasciotomy: as a tool for tissue recession in patients with plantar…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0672-2017·2016-12-14

    Mondelez Recalls Oreo Fudge Creme Cookies for Undeclared Milk Allergen

    Mondelez Global LLC is recalling Oreo Fudge Creme cookies (Original and Mint varieties) because milk is not declared on the ingredient list.

    Product
    Nabisco Oreo Fudge Creme Mint Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026967
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0701-2017·2016-12-14

    3M Recalls Universal Electrosurgical Pads Due to Unintended Material Defect

    3M is recalling Universal Electrosurgical Pads because an unintended process liner may impede the safe return of electrosurgical current, increasing the risk of patient burns.

    Product
    3M Universal Electrosurgical Pad, REF 9130 (100 pads / case) and 3M Universal Electrosurgical Pad with Cord, REF 9135-LP (40 pads / case) Product Usage: 3M Universal Electrosurgical Pads are designed to work with most electrosurgical unite (ESU) for virtually every…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0179-2017·2016-12-14

    North American Rescue Recalls K-9 Trauma Field Kits Due to Sterility Concerns

    North American Rescue LLC is recalling K-9 Trauma Field Kits because the manufacturer has concerns about the sterility of the included eye wash irrigating solution.

    Product
    K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V900000·2016-12-14

    Mercedes-Benz Recalls Vehicles for Potential Axle Bolt Fracture Risk

    Mercedes-Benz is recalling certain 2015-2016 models because axle bolts may not have been assembled correctly, potentially fracturing and causing vehicle instability.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ML250, AMG GL63, GL550, ML400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0180-2017·2016-12-14

    North American Rescue Recalls Amphibious Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling Amphibious Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.

    Product
    Amphibious Trauma Kit - Product Code 85-0639, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0175-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue LLC is recalling Range Trauma Kit Hardcases because the manufacturer has concerns about the sterility of the eye wash irrigating solution included in the kits.

    Product
    Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0609-2017·2016-12-14

    Calbee Recalls Black Pepper Green Pea Crisps Due to Undeclared Milk

    Calbee North America is recalling one lot of black pepper flavored green pea crisps because they may contain undeclared milk.

    Product
    HARVEST SNAPS, SNAPEA CRISPS, BLACK PEPPER FLAVORED GREEN PEA CRISPS, NET WT 3.3 OZ (93g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V899000·2016-12-14

    Mercedes-Benz Recalls Vehicles Due to Electric Power Steering Defect

    Mercedes-Benz is recalling specific 2013-2016 models because a steering control unit defect may cause loss of power steering assist or a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E350, S550, SL550, S600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0183-2017·2016-12-14

    North American Rescue Recalls USCG Boat Response Kits Due to Sterility Concerns

    North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.

    Product
    USCG Boat Response Kit - Product Code 80-0353, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide