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.

59351–59375 of 74011

  • HighFDA (Food)·F-1497-2014·2014-02-26

    El Encanto Recalls Hatch Valley XXXHot Salsa for Listeria Risk

    El Encanto, Incorporated is recalling specific lots of Bueno GC NM Hatch Valley XXXHot salsa due to possible Listeria monocytogenes contamination.

    Product
    Bueno GC NM Hatch Valley XXXHot 5-5# Z, Product Item Number 1020-3. Packaged in sealed poly film pouches. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size 5 units of 5 lbs each per case, totaling 25 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0990-2014·2014-02-26

    Perrigo Recalls Orbit Soft Infusion Sets Due to Connector Incompatibility

    Perrigo Diabetes Care is recalling Orbit soft Infusion sets because the luer-lock connectors are incompatible with standard infusion pumps.

    Product
    Orbit soft Infusion sets, 9 mm soft cannula, P10 (42") tubing; Single-Use Set Orbit Infusion Sets are sterile, non-pyrogenic, single-use devices intended to be used for subcutaneous delivery of medication , for example insulin, from an external infusion pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1529-2014·2014-02-26

    El Encanto Recalls Bueno GC NM Hatch Valley Mild Cheese

    El Encanto, Incorporated is recalling specific lots of Bueno GC NM Hatch Valley Mild cheese due to possible Listeria monocytogenes contamination.

    Product
    Bueno GC NM Hatch Valley Mild 2-12.5# Z, Product Item Number 1077-6. Packaged in sealed poly film pouches. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size of 2 units of 12.5 lbs. each per case, totaling 25 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1537-2014·2014-02-26

    NOW Foods Recalls Digestive Enzyme Capsules Due to Chloramphenicol Contamination

    NOW Foods is recalling digestive enzyme capsules because they may contain the antibiotic chloramphenicol. The recall covers 31,344 bottles distributed nationwide and in several foreign countries.

    Product
    Digestive enzyme capsules sold under the NOW Foods, Beeyoutiful, Best in Nature, Bluegrass Naturals Vitamin Company, Chicago Nutrition Company, Gluten-Free Remedies, Osa's Garden, and Professional Naturopathics brands and packaged in a plastic bottle containing 60 or 120…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1490-2014·2014-02-26

    El Encanto Recalls BACA'S GC Hot Salsa Due to Listeria Risk

    El Encanto, Incorporated is recalling BACA'S GC Hot 12-13oz Z due to possible Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    BACA'S GC Hot 12-13oz Z, Product Item Number 1010-0. Packaged in plastic containers. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size of 12 units of 13 oz each per case totaling 9.75 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1523-2014·2014-02-26

    El Encanto Autumn Roast Recalled for Possible Listeria Contamination

    El Encanto, Incorporated is recalling GC Autumn Roast Hot due to possible Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    GC Autumn Roast NO LABEL Hot 5-5# Z, Product Item Number 1062-0. Packaged in sealed poly film pouches. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size 5 units of 5 lbs each per case, totaling 25 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·14116·2014-02-26

    STX Recalls Shield Throat Protector Due to Laceration Hazard

    STX is recalling about 4,000 Shield throat protectors because the device can crack or break when struck by a lacrosse ball, posing a laceration hazard to the user's neck.

    Product
    STX Shield throat protector
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1505-2014·2014-02-26

    El Encanto Recalls Bueno GC NM Hot Salsa Due to Listeria Risk

    El Encanto, Incorporated is recalling specific lots of Bueno GC NM Hot 28oz salsa due to possible Listeria monocytogenes contamination.

    Product
    Bueno GC NM Hot 28oz, Product Item Number 1032-2. Packaged in plastic containers. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size of 6 units of 28 oz each per case totaling 10.5 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1504-2014·2014-02-26

    El Encanto Recalls SuperHot Product Due to Listeria Risk

    El Encanto, Incorporated is recalling specific lots of Bueno GC NM Hatch Valley Blakes SuperHot due to possible Listeria monocytogenes contamination.

    Product
    Bueno GC NM Hatch Valley Blakes SuperHot 5-5# Z, Product Item Number 1028-5. Packaged in sealed poly film pouches. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size 5 units of 5 lbs each per case, totaling 25 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1500-2014·2014-02-26

    El Encanto Organic Mild Cheese Recalled for Listeria Risk

    El Encanto, Incorporated is recalling Bueno GC Organic Mild cheese due to possible Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Bueno GC Organic Mild 12-13 oz Z, Product item Number 1023-1. Packaged in plastic containers. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size of 12 units of 13 oz each per case totaling 9.75 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1526-2014·2014-02-26

    El Encanto Recalls Bueno GC Strip Mild Cheese for Listeria Risk

    El Encanto, Incorporated is recalling Bueno GC Strip Mild cheese due to possible Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Bueno GC Strip Mild 2-12.5# Z, Product Item Number 1071-4. Packaged in double-poly bags.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1498-2014·2014-02-26

    El Encanto Recalls Bueno GC NM XHot for Listeria Risk

    El Encanto, Incorporated is recalling Bueno GC NM XHot due to possible Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Bueno GC NM XHot 12-13 oz Z, Product Item Number 1021-1. Packaged in plastic containers. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size of 12 units of 13 oz each per case totaling 9.75 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1532-2014·2014-02-26

    El Encanto Recalls Bueno GC NM Mild Cheese for Listeria Risk

    El Encanto, Incorporated is recalling Bueno GC NM Mild cheese due to possible Listeria monocytogenes contamination. The product was distributed nationwide.

    Product
    Bueno GC NM Mild 2-12.5# Z, Product Item Number 1093-3. Packaged in sealed poly film pouches. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size of 2 units of 12.5 lbs. each per case, totaling 25 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1507-2014·2014-02-26

    El Encanto Recalls Bueno GC NM Hot Salsa Due to Listeria Risk

    El Encanto, Incorporated is recalling specific lots of Bueno GC NM Hot 6-56oz Z salsa due to possible Listeria monocytogenes contamination.

    Product
    Bueno GC NM Hot 6-56oz Z, Product Item Number 1042-2. Packaged in plastic containers. All packed in cardboard shipper box that is then sealed with attached shipper label. Total package size of 6 units of 56 oz each per case totaling 21 lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1044-2014·2014-02-26

    Zimmer Recalls Self-Tapping Cortical Screws Due to Packaging Validation Issues

    Zimmer is recalling 7 million self-tapping cortical screws because packaging operations at a Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    3.5 X 10 CORT SCREW SELFT 3.5 X 12 CORT SCREW SELFT 3.5 X 14 CORT SCREW SELFT 3.5 X 16 CORT SCREW SELFT 3.5 X 18 CORT SCREW SELFT 3.5 X 20 CORT SCREW SELFT 3.5 X 22 CORT SCREW SELFT 3.5 X 24 CORT SCREW SELFT 3.5 X 26 CORT SCREW SELFT 3.5 X 28 CORT SCREW SELFT 3.5 X 30…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1005-2014·2014-02-26

    Zimmer Recalls Versa-FX II Knee Implants Due to Packaging Validation Issues

    Zimmer is recalling Versa-FX II knee implants because packaging operations at a Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    VERSA-FX II KEYLESS TUBE, VERSA-FX II KEYLESS SHORT, VERSA-FX II SHORT TUBE PL, VERSA-FX II STD TUBE PLAT and VERSA-FX II SUPRACONDYLR Item codes starting with 0011930, 0011931 and 0011941
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1043-2014·2014-02-26

    Zimmer Recalls 3.5 Compression Plates Due to Packaging Validation Issues

    Zimmer is recalling 3.5 compression plates sterile packaged at its Puerto Rico facility because packaging operations were not properly validated, despite passing seal integrity tests.

    Product
    3.5 COMP PLT, 4 HOLE 3.5 COMP PLT, 5 HOLE 3.5 COMP PLT, 6 HOLE 3.5 COMP PLT, 8 HOLE 3.5 COMP PLT, 9 HOLE 3.5 COMP PLT, 10 HOLE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2014·2014-02-26

    Zimmer Recalls Sterile Orthopedic Screws Due to Packaging Validation Issues

    Zimmer is recalling 7 million sterile orthopedic screws because packaging operations at its Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.

    Product
    1.5 X 6 CORT SCREW HEX/SE 2.0 X 6 CORT SCREW HEX/SE 2.0 X 10 CORT SCREW CRUCI 2.0 X 12 CORT SCREW CRUCI 2.0 X 14 CORT SCREW CRUCI 2.0 X 16 CORT SCREW HEX/S 2.0 X 16 CORT SCREW CRUCI 2.0 X 18 CORT SCREW CRUCI 2.0 X 20 CORT SCREW CRUCI 2.0 X 26 CORT SCREW CRUCI 2.0 X 28…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1034-2014·2014-02-26

    Zimmer Recalls 6 Degree COCR Femoral Heads Due to Packaging Validation Issues

    Zimmer is recalling 6 Degree COCR Femoral Heads because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    6 DEGREE COCR FEM HEAD 36
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1003-2014·2014-02-26

    Zimmer Recalls Free-Lock Orthopedic Devices Due to Packaging Validation Issues

    Zimmer is recalling specific Free-Lock orthopedic devices because packaging operations at a Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    FREE-LOCK LAG SCREW, 12.7, FREE-LOCK LAG SCREW, 15.8, FREE-LOCK SUPRACOND TUBE and FREE-LOCK TUBE & SCP PLAT. Items starting with codes 0011810 and 0011811.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1008-2014·2014-02-26

    Zimmer Recalls Sterile Orthopedic Screws and Nails Due to Packaging Validation Issues

    Zimmer is recalling specific sterile orthopedic screws and nails because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    RECON SCREW LG 5.5MM DIA and M/DN FEM IM NAIL 8MM DIA to 16 MM DIA. Item codes starting with 0022520, 0022521, 002522, 0022523, 0022524 and 0022525.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1011-2014·2014-02-26

    Zimmer Recalls Humeral Intramedullary Nails Due to Packaging Validation Issues

    Zimmer is recalling 7,044,680 humeral intramedullary nails because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    M/DN HUMERAL I/M NAIL. Sizes from 6 MM to 13 MM. Codes starting with 0022541, 002542 and 0022543.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1029-2014·2014-02-26

    Zimmer Recalls Versys Femoral Stems Due to Packaging Validation Issues

    Zimmer is recalling Versys femoral stems because packaging operations at its Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.

    Product
    12/14 UNIPOLAR FEMORAL HE VERSYS CEM LD/FX SZ 11X12 VERSYS CEM LD/FX SZ 12X12 VERSYS CEM LD/FX SZ 14X13 VERSYS CEM LD/FX SZ 16X14 VERSYS CEM LD/FX ST 18X15 VERSYS PRESS FIT LD/FX ST VERSYS PRESS FIT LD/FX SZ VERSYS ADVOCATE CEMENTED VERSYS ADVOCATE V-LIGN CE VERSYS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1018-2014·2014-02-26

    Zimmer Recalls Modular Austin Moore Femoral Neck Implants Due to Packaging Validation

    Zimmer is recalling Modular Austin Moore Femoral Neck implants because packaging operations at a Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.

    Product
    MODULAR AUSTIN MOORE FENE. Item codes starting with 45502001, 455503001 and 455504001
    Category
    Medical Device
    Distribution
    Distributed nationwide