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.

43726–43750 of 73984

  • HighFDA (Devices)·Z-1861-2017·2017-04-26

    Zimmer Biomet Recalls Polyethylene Knee Implants Due to Endotoxin Levels

    Zimmer Biomet is recalling 28,253 polyethylene knee implants because endotoxin levels exceeded process maximum limits. The affected products were distributed worldwide.

    Product
    various polyethylene implants Knees Revision Tibial Tray Systems Oxford Partial Knee Orthopedic Salvage System Vanguard Complete Knee System Vanguard SSK Revision System Biomet Patella Maxim Complete Knee System Biomet Series A Patella Vanguard 360 Revision System…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1847-2017·2017-04-26

    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 10MM Product Number: 72204046 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-1845-2017·2017-04-26

    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 9MM Product Number: 72204044 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-1858-2017·2017-04-26

    Zimmer Biomet Recalls Polyethylene Implants Due to High Endotoxin Levels

    Zimmer Biomet is recalling BIO PLUG 10MM polyethylene implants because endotoxin levels exceeded process maximum limits.

    Product
    various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight bearing accessory. Sterile, optional speciality components that are non-bioabsorbable, implantable devices designed to be inserted into the medullary canal of a bone during orhtopedic surgery to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1834-2017·2017-04-26

    Signal Medical Soft Face Mallet Recalled for Tip Detachment Risk

    Signal Medical Corporation is recalling 1,640 Soft Face "No Bounce" Mallets because the poly tip may detach during use, posing a risk of foreign material in the surgical field.

    Product
    Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1868-2017·2017-04-26

    FDA Recalls 84 Zimmer CAS SmartTools Knee System Instruments

    Orthosoft, Inc. dba Zimmer CAS is recalling 84 SmartTools Knee System Orthopedic Stereotaxic Instruments due to complaints of bent or broken Drive Pins.

    Product
    SmartTools Knee System Orthopedic Stereotaxic Instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1859-2017·2017-04-26

    Zimmer Biomet Recalls Polyethylene Implants Due to High Endotoxin Levels

    Zimmer Biomet is recalling 28,253 polyethylene implants for shoulder and elbow replacements because endotoxin levels exceeded process maximum limits.

    Product
    various polyethylene implants Extremities, Shoulders and Elbows BioModular Shoulder System; Comprehensive Shoulder System; Comprehensive Reverse Shoulder System Product Usage: Shoulder Replacement Elbow Replacement
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1860-2017·2017-04-26

    Zimmer Biomet Recalls Polyethylene Hip Implants Due to Endotoxin Levels

    Zimmer Biomet is recalling 28,253 polyethylene hip implant components worldwide because endotoxin levels exceeded process maximum limits.

    Product
    various polyethylene implants Hips Active Articulation ArComXL Bearings Active Articulation E1 Bearings Arcos Taper Cap BIOLOX delta Option Head E1 RingLoc Bi-Polar Freedom Constrained Liner +5mm Hi-Wall ArcomXL All Poly Rimloc E1 10 Degree Liner RingLoc +3mm Hi-Wall…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1993-2017·2017-04-26

    Dawn Food Products Recalls Sheila G's Eggless Brownie Brittle Mix

    Dawn Food Products is recalling Sheila G's Eggless Brownie Brittle Mix because it contains ingredients recalled for potential Salmonella contamination.

    Product
    SHEILA G'S EGGLESS BROWNIE BRITTLE MIX Item 02403038 50 lb bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1862-2017·2017-04-26

    Zimmer Biomet Recalls Polyethylene Implants Due to High Endotoxin Levels

    Zimmer Biomet is recalling 28,253 custom polyethylene implants because endotoxin levels exceeded process maximum limits. The affected parts were distributed worldwide.

    Product
    various polyethylene implants Custom parts Product Usage: Custom
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1836-2017·2017-04-26

    Valleylab Laparoscopic Handset Recalled for Activation Button Failure

    COVIDIEN MEDTRONIC is recalling Valleylab Laparoscopic Handsets because customer reports indicate the device may continue operating after the activation button is released.

    Product
    Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V275000·2017-04-26

    Nissan Recalls 2017 Versa Models Due to Passenger Air Bag Defect

    Nissan is recalling 2017 Versa and Versa Note vehicles because the passenger air bag ring plate may fail, causing improper deployment and increasing injury risk.

    Product
    NISSAN — NISSAN VERSA, VERSA NOTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1863-2017·2017-04-26

    Zimmer Biomet Recalls Polyethylene Implants Due to High Endotoxin Levels

    Zimmer Biomet is recalling Repicci II Tibial Components for partial knee replacement because endotoxin levels exceeded process maximum limits.

    Product
    various polyethylene implants Sports Med Repicci II Tibial Components Product Usage: Partial knee replacement
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1849-2017·2017-04-26

    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 11MM Product Number: 72204048 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0676-2017·2017-04-26

    Taro Recalls Nystatin and Triamcinolone Acetonide Cream for Stability Failures

    Taro Pharmaceuticals is recalling Nystatin and Triamcinolone Acetonide Cream because it failed content uniformity specifications during 18-month stability testing.

    Product
    NYSTATIN AND TRIAMCINOLONE ACETONIDE — NYSTATIN AND TRIAMCINOLONE ACETONIDE (NYSTATIN AND TRIAMCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1837-2017·2017-04-26

    Alcon Recalls Patient Care Kits Due to Sterile Packaging Concerns

    Alcon is voluntarily removing 561,702 Patient Care Kits from the US market because the supplier reported potential sterile packaging compromise.

    Product
    Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medical professionals for specific procedures. The Patient Care kits are configured with customer-specific components
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1856-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Orthopedic Screws Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 100 units of D-RAD orthopedic screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.

    Product
    D-RAD, 2.4MMX 20MM, S.T. CORTEX SCREW, QTY: (1), STERILE R, RES 74682420 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1852-2017·2017-04-26

    Verathon Recalls GVL 2 Stat Blades Packaged with Incorrect Size

    Verathon is recalling GVL 2 Stat blades (lot GC32825) because they were physically packaged with the incorrect size device, GVL 1 Stat blades.

    Product
    It is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg). Part Number 0270-0429: GVL 2 Stat (box of 10 Stats). Part Number 0574-0027: GVL 2 Stat (single pouched Stat). Part Number 0270-0662: GlideScope AVL Video Baton 1-2 Kit (where one box of 10, part…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1828-2017·2017-04-26

    Merge Healthcare Recalls Eye Station and Eye Care PACS Software

    Merge Healthcare is recalling Eye Station and Eye Care PACS software because antivirus programs may permanently delete newly captured medical images.

    Product
    Merge Eye Station and Merge Eye Care PACS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1857-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Locking Screws Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 197 units of D-RAD locking screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.

    Product
    D-RAD, S.T. LOCKING SCREWS, T7, QTY: (1), STERILE R, in the following sizes: (a) 2.4MM X 10MM, RES 74692410 (b) 2.4MM X 12MM, RES 74692412 (c) 2.4MM X 16MM, RES 74692416 (d) 2.4MM X 22MM, RES 74692422 (e) 2.4MM X 24MM, RES 74692424
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1855-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Locking Pegs Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 19 units of D-RAD locking pegs because the expiration dates on the labels are incorrect and later than the actual dates.

    Product
    D-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1854-2017·2017-04-26

    Smith & Nephew Recalls Peri-Loc VLP Self-Tapping Cortex Screws Due to Labeling Error

    Smith & Nephew is recalling specific Peri-Loc VLP self-tapping cortex screws because the expiration dates printed on the labels are incorrect and later than the actual dates.

    Product
    Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide