The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

60651–60675 of 74011

  • HighFDA (Drugs)·D-094-2014·2013-12-11

    Main Street Compounding Pharmacy Recalls Estradiol Pellets Due to Adverse Reactions

    Main Street Family Pharmacy is recalling Estradiol Pellets 31mg after receiving reports of skin abscesses linked to a different compounded product.

    Product
    Estradiol Pellets 31mg, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-325-2014·2013-12-11

    Badger Kids Sunscreen Recalled for Microbial Contamination

    W.S. Badger Company is recalling specific lots of Badger Kids Sunscreen Lotion due to microbial contamination. The product was distributed in the US, Canada, and several other countries.

    Product
    Badger Kids Broad Spectrum SPF30 Zinc Oxide Sunscreen Lotion Tangerine & Vanilla, 4 fl. oz.. Tube, UPC Code: 634084490145 (US), UPC code: 634084490169 (Canada)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0453-2014·2013-12-11

    Sunrise Zippie Voyage Stroller Recalled for Potential Seat Dislodgement

    Sunrise Medical is recalling Zippie Voyage strollers because a plastic latch may deform, allowing the seat to dislodge and causing the occupant to slide out.

    Product
    Sunrise Brand Zippie Voyage, Chair with Casters, Early Intervention Device (Stroller), Model: EIZ14; Product is manufactured and distributed by Sunrise Medical (US) LLC., Fresno, CA. Used by a person to move from one place to another while sitting.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0442-2014·2013-12-11

    Boston Scientific Recalls Navigator HD Ureteral Access Sheath Sets

    Boston Scientific is recalling 449 units of Navigator HD Ureteral Access Sheath Sets because the dilator tip may separate from the body.

    Product
    Navigator HD l3F/15F x 46cm Ureteral Access Sheath Set Product No M0062502280, RDF Catalog M0062502290, Sterile. Indicated for use in endoscopic procedures to facilitate the passage of endoscopes, urological instruments and for the injection of fluids into the urinary tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14049·2013-12-11

    Solowave Recalls Tornado Tube Slides Due to Laceration Hazard

    Solowave is recalling Tornado brand home playground tube slides because plastic port holes can break and cut children. About 20,700 units were sold in the U.S. and Canada.

    Product
    Tornado brand home playground tube slides with port holes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0455-2014·2013-12-11

    Synthes Zero-P VA Implant Recalled for Potential Screw Back-Out Risk

    Synthes USA is recalling specific Zero-P VA implants because a screw could back out if the blocking mechanism is not visually confirmed to cover the screw head.

    Product
    Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Synthes Zero-P VA Implant 7 MM Height Parallel Sterile is a stand alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0436-2014·2013-12-11

    Intuitive Surgical Recalls da Vinci Patient Side Manipulator Assemblies

    Intuitive Surgical is recalling 1,386 da Vinci Patient Side Manipulator assemblies due to friction that can cause instrument motion to stall and catch up.

    Product
    Assembly, Patient Side Manipulator on da Vinci Surgical Systems: da Vinci S Surgical System; da Vinci SI Surgical System da Vinci Si-e Surgical System; Manufactured by Intuitive Surgical Sunnyvale, CA 94086. The Intuitive Surgical Endoscopic Instrument Control System…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0440-2014·2013-12-11

    Boston Scientific Recalls Navigator HD Ureteral Access Sheath Sets

    Boston Scientific is recalling 274 units of Navigator HD Ureteral Access Sheath Sets because the dilator tip may separate from the body.

    Product
    Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No M0062502270, RDF Catalog No 250-227, Sterile. Indicated for use in endoscopic procedures to facilitate the passage of endoscopes, urological instruments and for the injection of fluids into the urinary tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V615000·2013-12-11

    GM Recalls 2012-2013 Silverado and Sierra HD Diesel Trucks

    General Motors is recalling 2012-2013 Chevrolet Silverado HD and GMC Sierra HD diesel trucks because a fuel transfer pump malfunction could cause the vehicle to stall unexpectedly.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO, SIERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0433-2014·2013-12-11

    Siemens syngo Lab Data Manager Software Recall for Auto-verification Failures

    Siemens Healthcare Diagnostics is recalling syngo Lab Data Manager software versions VA11B and VA12A because the system may release results that require manual review or delay result transmission.

    Product
    syngo(R) Lab Data Manager - Version VA11B and VA12A Systems Securely consolidates data from multiple lab instruments, the LIS and Siemens StreamLAB(R) Automation Solutions. It provides autoverification, integrated QC capabilities, browser-based connectivity supporting up to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0432-2014·2013-12-11

    Olympus Recalls Thunderbeat Surgical Instruments Due to Component Damage

    Olympus America Inc. is recalling Thunderbeat surgical instruments because they may crack, break, or deform during use.

    Product
    TB-0545PC: THUNDERBEAT 5 mm , 45 em, Pistol Grip TB-0535PC: THUNDERBEAT 5 mm, 35 em, Pi stol Grip TB-0545IC: THUNDERBEAT 5 mm, 45 em, In line Grip TB-0535IC: THUNDERBEAT 5 mm, 35 em, Inline Grip TB-0520IC: THUNDERBEAT 5 mm, 20 em, In line Grip TB-051 OIC: THUNDERBEAT 5 mm, I 0…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0431-2014·2013-12-11

    Philips Easy Diagnost Eleva Fluoroscopic Software Recall

    Philips Medical Systems is recalling 19 Easy Diagnost Eleva devices because they were delivered with outdated application software.

    Product
    Easy Diagnost Eleva Universal Fluoroscopic applications
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0435-2014·2013-12-11

    CareFusion Recalls VersaSafe Extension Sets Due to Adhesive Defect

    CareFusion is recalling VersaSafe Extension Sets because excessive adhesive may prevent the male spin collar from operating as intended.

    Product
    VersaSafe Extension Set, Model No. 21000M-007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0439-2014·2013-12-11

    Varian Medical Systems Recalls C-Series Linear Accelerators for Software Correction

    Varian Medical Systems is recalling 3,809 C-Series linear accelerators to install a software solution that corrects a previous issue.

    Product
    C-Series: Clinac, Trilogy, Trilogy Tx. , Novalis high energy linear accelerators and UNIQUE single energy linear accelerator; Versions 7, 8 and 9. The UNIQUE is not sold in the US. Product Usage: The Varian High Energy Linear Accelerator is indicated for stereotactic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0434-2014·2013-12-11

    Advanced Sterilization Products Recalls SteriTite Containers Due to Sterility Assurance Concerns

    Advanced Sterilization Products is recalling SteriTite containers because data does not consistently show that the required sterility assurance level is achieved during testing.

    Product
    STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" high, product code: 13902; STERITITE Mini Mid Size, 3" high, product code: 13903; STERITITE Container Kit, 1/2 size, 4" high, product code: 13904; STERITITE Container Kit, 3/4 size, 4" high, product code: 13905…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0430-2014·2013-12-11

    Siemens Dimension Vista Diagnostic Vials Recalled for Volume Error

    Siemens is recalling Dimension Vista 500 and 1500 reloaded vials because they may incorrectly reset to full volume, potentially affecting diagnostic accuracy.

    Product
    Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Vials - limited to systems using software versions 3.4 and 3.5.1. Diagnostic device intended to determine a variety of analytes in human body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0429-2014·2013-12-11

    Synthes Soft Tissue Retractor Recalled for Locking Nut Malfunction

    Synthes USA HQ, Inc. is recalling 374 units of the Small Extendible Soft Tissue Retractor due to a locking nut malfunction.

    Product
    Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates easy preparation of the epipereosteal cavity for percutaneous plate insertion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-324-2014·2013-12-11

    Badger Baby Sunscreen Recalled for Microbial Contamination

    W.S. Badger Company Inc. is recalling specific lots of Badger Baby and Kids Sunscreen Lotion due to microbial contamination.

    Product
    Badger Baby Broad Spectrum SPF 30 Zinc Oxide Sunscreen Lotion Chamomile & Calendula, 4fFl.oz Tube, UPC code: 634084490091 (US) UPC Code: 634084490114 (Canada)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14045·2013-12-10

    Exmark Recalls Commercial Walk-Behind Mowers Due to Blade Injury Hazard

    Exmark is recalling 2013 Commercial 30-inch Walk-Behind Mowers because the blade can break and injure users. Consumers should stop using the mowers and contact Exmark for a free repair.

    Product
    Commercial Walk-Behind Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14047·2013-12-10

    efco Gas Trimmers Recalled by CPSC Due to Fire Hazard

    Emak USA is recalling efco gas trimmers because the engine muffler can break and cause a fire. Consumers should stop using them and return them for a free repair.

    Product
    efco brand Gas Trimmers from Emak USA
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14048·2013-12-10

    PackTite Recalls Bed Bug Heating Units Due to Fire Hazard

    PackTite is recalling approximately 9,000 bed bug heating units because they can overheat, melt, and cause fires. No injuries have been reported.

    Product
    PackTite™ Heating Units for Bed Bug Control
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14044·2013-12-09

    Linear Recalls PERS Transmitters Due to Battery Signal Failure

    Linear is recalling about 48,000 Personal Emergency Reporting System transmitters because battery clips can corrode, causing the devices to fail without warning.

    Product
    Personal Emergency Reporting System (PERS) Transmitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V652000·2013-12-09

    Skyline Recalls 2006-2013 Trailers Due to Door Lock Jamming Risk

    Skyline is recalling 2006-2013 travel and fifth-wheel trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.

    Product
    SKYLINE — SKYLINE SKYCAT, WEEKENDER, NOMAD, MOUNTAINVIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V637000·2013-12-09

    Marathon Recalls 2006-2013 Trailers Due to Door Lock Jamming Risk

    Marathon Homes is recalling 2006-2013 towable and fifth wheel travel trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside.

    Product
    MARATHON — MARATHON TOWABLE TRAILER/5TH WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide