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.

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.

43701–43725 of 73984

  • HighNHTSA·17V286000·2017-04-27

    Jaguar Recalls 2017 XE Diesel Vehicles for Fuel Hose Leak

    Jaguar is recalling 2017 XE vehicles with 2.0L diesel engines because a fuel return hose may leak, creating a skid hazard or fire risk.

    Product
    JAGUAR — JAGUAR XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1991-2017·2017-04-26

    Dawn Food Products Recalls R&H Speedy Creme Vanilla Filling Mix

    Dawn Food Products Inc. is recalling R&H Speedy Creme Vanilla Filling Mix because it contains ingredients recalled for potential Salmonella contamination.

    Product
    R&H Speedy Creme Vanilla Filling Mix Item 01148908 25 pound bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1821-2017·2017-04-26

    Philips UNIQ X-ray Systems Recalled for Potential Fire Hazard

    Philips is recalling UNIQ X-ray systems because a leak in the detector cooling system could cause liquid to drip onto electrical components, potentially leading to fire.

    Product
    UNIQ: UNIQ FD10 722026; UNIQ FD10/10 722027; UNIQ FD20/10 biplane 722029; UNIQ FD10 OR Table 722033; UNIQ FD10/10 OR Table 722034; UNIQ FD20/10 OR Table 722036; UNIQ FD20/20 722038; UNIQ FD20/20 biplane OR Table 722039
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1839-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM Product Number: 72204038 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1844-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: 72204043 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1843-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recalled for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: 72204042 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1838-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM Product Number: 72204037 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1990-2017·2017-04-26

    Dawn Food Products Recalls Vanilla Pudding Mix for Salmonella Risk

    Dawn Food Products is recalling R&H Vanilla Speedy Creme Instant Pudding and Pie Filling Mix because it contains ingredients recalled for potential Salmonella contamination.

    Product
    R&H VANILLA Speedy Creme Instant Pudding and Pie Filling Mix Item 00727521 4 lbs 2 oz retail paper bag, six retail bags per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1842-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recalled for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills due to a potential for the cutting blade to detach or the drill head to fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: 72204041 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1840-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: 72204039 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1820-2017·2017-04-26

    Philips Recalls Allura Xper Systems Due to Chiller Leak Fire Risk

    Philips is recalling specific Allura Xper medical imaging systems because a leak in the detector cooling system could cause liquid to drip onto electrical components, potentially leading to fire.

    Product
    Allura Xper Release 8.2 (Laird chiller is always installed); Allura Xper FD10 722026; Allura Xper FD10/10 722027; Allura Xper FD20/10 biplane 722029; Allura Xper FD10 OR Table 722033; Allura Xper FD10/10 OR Table 722034; Allura Xper FD20/10 OR Table 722036; Allure Xper FD20/20…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1846-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number: 72204045 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1851-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: 72204050 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1992-2017·2017-04-26

    Dawn Food Products Recalls Chocolate Pudding Mix for Salmonella Risk

    Dawn Food Products Inc. is recalling R&H Chocolate Speedy Creme Instant Pudding and Pie Filling Mix because it contains ingredients recalled for potential Salmonella contamination.

    Product
    R&H CHOCOLATE Speedy Creme Instant Pudding and Pie Filling Mix Item 00257857 4 lbs 2 oz retail paper bag, six retail bags per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1841-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills due to a potential for the cutting blade to detach or the drill head to fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: 72204040 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1822-2017·2017-04-26

    Philips Allura Xper Systems Recalled for Chiller Leak Fire Risk

    Philips is recalling specific Allura Xper systems equipped with Laird chillers because a leak in the cooling system could cause liquid to drip onto electrical components, potentially leading to fire.

    Product
    The following systems are only affected if a Laird chiller is installed (11NC: 98960021599): Allura Xper Releases 3 to 8.1: Allura Xper FD10 (C+F). 722003; Allura Xper FD10/10 722005; Allura Xper FD20 722006; Allura Xper FD20/10 and FD20/20 722008; Allura Xper FD10 722010…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V279000·2017-04-26

    Polaris Recalls 2016-2017 GEM Electric Vehicles for Loose Lug Nuts

    Polaris is recalling 2016-2017 GEM E2, E4, E6, and ELXD electric vehicles because front wheel lug nuts may loosen, potentially causing a wheel to detach.

    Product
    GEM — GEM E2, E6, E4, ELXD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1848-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM Product Number: 72204047 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1989-2017·2017-04-26

    Dawn Food Products Recalls Vanilla Powdered Filling for Salmonella Risk

    Dawn Food Products is recalling Quik 'n Creamy Vanilla Powdered Filling because it contains ingredients recalled for potential Salmonella contamination.

    Product
    QUIK 'N CREAMY VANILLA POWDERED FILLING Item number 00014100 25 pound bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1850-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11.5MM Product Number: 72204049 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1869-2017·2017-04-26

    Elcam Minimal Residual Volume Stopcock Recalled for Punctures

    Elcam Medical, Inc. is recalling 810 units of Minimal Residual Volume Luer-activated Swabable-stockcock devices found to have punctures.

    Product
    Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w gxl:w1/r rbls Product Usage: indicated for fluid flow directional control and for providing access ports for administration of intravenous solutions. Typical uses include pressure monitoring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V278000·2017-04-26

    Elgin Street Sweepers Recalled for Detaching Broom Flap Support End Cap

    Elgin is recalling 2016-2017 Broom Bear, Eagle, and Road Wizard street sweepers because the main broom flap support end cap may detach, creating a road hazard.

    Product
    ELGIN — ELGIN BROOM BEAR, EAGLE, ROAD WIZARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1873-2017·2017-04-26

    Laerdal Compact Suction Unit 4 Recalled for Electronic Component Damage

    Laerdal Medical Corporation is recalling 4,377 Compact Suction Unit 4 devices because an electronic component may be damaged, potentially affecting the On/Off functionality.

    Product
    Laerdal Compact Suction Unit ¿ 4 under the following labels: 1) 300 ml (3.3 lbs) canister version - CATALOG #(s): 88006101 - LCSU 4, 300 ml Complete unit (US), 88006103 - LCSU 4, 300 ml Complete unit (UK), 88006140 - LCSU 4, 300 ml Complete unit (EUR), 881151 - Replacement unit…
    Category
    Medical Device
    Distribution
    Distributed nationwide