The Recall Desk

State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53801–53825 of 74002

  • HighFDA (Devices)·Z-1642-2015·2015-05-27

    DeRoyal Specimen Retrieval Bags Recalled for Tearing During Use

    DeRoyal Industries is recalling 5,359 Medium Specimen Retrieval Bags because they may tear or come apart during laparoscopic procedures.

    Product
    DeRoyal(R) Medium Specimen Retrieval Bag, REF 5500-000-003, Rx Only Product Usage: The device is a single-use specimen retrieval bag indicated for use in laparoscopic procedures to capture and remove organs or tissue from the body cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1622-2015·2015-05-27

    Roche Homocysteine Test System Recalled for Inaccurate Low Results

    Roche Diagnostics is recalling Homocysteine Reagent lots due to complaints of under-recovery and falsely low patient results, which could delay diagnosis of peripheral vascular disease.

    Product
    Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA Homocysteine Enzymatic Assay is an in vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V315000·2015-05-27

    Toyota Recalls 2015 Tundra for Incorrect Tire Pressure Placard

    Southeast Toyota Distributors is recalling 144 model year 2015 Toyota Tundra vehicles because the tire placard lists incorrect inflation pressure, which could lead to underinflation and tire failure.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1640-2015·2015-05-27

    Richard-Allan Scientific Recalls Mucolexx Mucolytic Agent Due to Fungal Contamination

    Richard-Allan Scientific is recalling Mucolexx mucolytic agent and Mucolexx products after a customer reported fungal contamination in two lots.

    Product
    Lerner Laboratories Mucolexx, 1 pint / 473 ml & 1 gallon/3.8 L; Shandon Mucolexx 500ml/0.13gal, 4L/1.06 gal, 120mL Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1634-2015·2015-05-27

    Stryker Scorpio femoral component recall due to blister seal strength

    Stryker Howmedica Osteonics is recalling 1,147 Scorpio femoral components because the inner blister peel strength may be below validated requirements, potentially affecting sterile barrier shelf life.

    Product
    Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1635-2015·2015-05-27

    Stryker Triathlon Femoral Component Recalled for Sterile Barrier Seal Issues

    Stryker Howmedica Osteonics is recalling 1,147 Triathlon femoral components because the inner blister seal strength may be below validated requirements, potentially affecting sterile shelf life.

    Product
    Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1633-2015·2015-05-27

    Stryker Howmedica Hip Prosthesis Components Recalled for Seal Defects

    Stryker Howmedica is recalling 1,147 RESTORATION Acetabular Augment System components because the inner blister seal strength may be below validated requirements, potentially affecting sterile shelf life.

    Product
    Stryker Howmedica Osteonics RESTORATION Acetabular Augment System; Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. Hip prosthesis component. The RESTORATION Acetabular Wedge Augments provide multiple options to address the wide range of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1626-2015·2015-05-27

    Wright Medical Recalls Phalinx Hammertoe Handles Due to Incorrect Laser Etching

    Wright Medical Technology is recalling 124 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.

    Product
    PHALINX (TM) HAMMERTOE HANDLE, SIZE: MEDIUM, STYLE: ANGLED, REF 45304013, CONTENTS 1 EACH, RX ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1627-2015·2015-05-27

    Wright Medical Recalls PHALINX Hammertoe Handles Due to Incorrect Laser Etching

    Wright Medical Technology is recalling 126 units of PHALINX Hammertoe Handles because the term 'DORSAL' was laser etched on the incorrect side.

    Product
    PHALINX (TM) HAMMERTOE HANDLE, SIZE: LARGE, STYLE: ANGLED, REF 45304014, CONTENTS 1 EACH, RX ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1554-2015·2015-05-27

    Philips DigitalDiagnost X-Ray System Recalled for Missing Exposure Beep Signal

    Philips Medical Systems is recalling 54 DigitalDiagnost X-Ray systems because they fail to emit a beep signal after exposure if powered on for over 12 hours.

    Product
    Philips Healthcare DigitalDiagnost System X-Ray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1625-2015·2015-05-27

    Wright Medical Recalls Phalinx Hammertoe Handle Due to Incorrect Etching

    Wright Medical Technology is recalling 121 units of Phalinx Hammertoe Handles because the word 'DORSAL' was laser-etched on the incorrect side.

    Product
    PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012, CONTENTS 1 EACH, RX ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1555-2015·2015-05-27

    Philips DuraDiagnost X-Ray System Recalled for Missing Exposure Beep

    Philips Medical Systems is recalling DuraDiagnost X-ray systems because they may fail to emit a termination beep after 12 hours of operation, violating safety regulations.

    Product
    Philips Healthcare DuraDiagnost X- Ray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1624-2015·2015-05-27

    Wright Medical Recalls Phalinx Hammertoe Handles Due to Incorrect Laser Etching

    Wright Medical Technology is recalling 126 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.

    Product
    PHALINX (TM) HAMMERTOE HANDLE, SIZE: X-SMALL, STYLE: ANGLED, REF 45304011, CONTENTS 1 EACH, RX ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1083-2015·2015-05-27

    Mylan Recalls Fexofenadine Hydrochloride Tablets Due to Impurity Levels

    Mylan Institutional, Inc. is recalling 1,363 cartons of Fexofenadine Hydrochloride 60 mg tablets because routine stability testing showed slightly above specification results for a related compound.

    Product
    Fexofenadine Hydrochloride Tablets, USP 60 mg, Allergy, Non-Drowsy, Antihistamine, 100 tablets (10 X 10) per UD Cartons, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505, USA, NDC 51079-547-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1630-2015·2015-05-27

    CooperSurgical Recalls Carter-Thomason II Port Closure System Due to Printing Defect

    CooperSurgical is recalling 430 units of the Carter-Thomason II Port Closure System because pad printing on the suture guide may flake off.

    Product
    Carter-Thomason II Port Closure System; Model Number(s) CTI-1015P, for use in endoscopic and laparoscopic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalNHTSA·15V313000·2015-05-26

    Chrysler Recalls Vehicles Due to Driver Air Bag Inflator Rupture Risk

    Chrysler is recalling specific 2004-2011 Dodge, Chrysler, and Mitsubishi vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    RAM — RAM, CHRYSLER, DODGE redundant 5500, redundant 4500, 300, RAM 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V310000·2015-05-26

    PACCAR Recalls Kenworth and Peterbilt Trucks for Driveshaft Weld Failure

    PACCAR is recalling specific Kenworth and Peterbilt trucks because a driveshaft weld may fail due to corrosion, potentially causing loss of power to the rear wheels.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 587, T660, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V312000·2015-05-26

    Dodge Ram Trucks Recalled for Air Bag Inflator Rupture Risk

    Chrysler is recalling 2003 Dodge Ram trucks because the passenger air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    DODGE — DODGE RAM 3500, RAM 2500, RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V309000·2015-05-26

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Fire Risk

    PACCAR is recalling specific Kenworth and Peterbilt trucks because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.

    Product
    PETERBILT — PETERBILT, KENWORTH 365, 384, 348, 382
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V308000·2015-05-26

    Open Range Recalls 2015 Fifth Wheel Trailers Due to Step Rivet Failure

    Open Range R.V. Company is recalling 122 model year 2015 Roamer, Mesa Ridge, and 3X fifth wheel trailers because a rivet on the entry steps may shear, causing the steps to fail.

    Product
    OPEN RANGE — OPEN RANGE 3X, ROAMER, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15149·2015-05-26

    BRP Recalls Youth Can-Am ATVs for Federal Standard Violations

    Bombardier Recreational Products is recalling about 12,500 youth Can-Am ATVs because they fail to meet federal speed and parking brake requirements, posing a crash hazard.

    Product
    All-terrain vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15148·2015-05-26

    Gerber Recalls Cohort Folding Knives Due to Laceration Hazard

    Gerber is recalling Cohort folding knives because the locking mechanism can fail, posing a laceration hazard. Six injuries have been reported.

    Product
    Cohort Folding Knife
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V307000·2015-05-26

    Collins Recalls 2015 School Buses for Seat Flammability Defect

    Collins Bus Corporation is recalling 13 model year 2015 school buses because seat foam may not meet federal flammability standards, increasing fire risk.

    Product
    COLLINS — COLLINS DH500, SH40, SL408, DE516WR
    Category
    Vehicle
    Distribution
    Distributed nationwide