The Recall Desk

State

US Virgin Islands product recalls

73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27126–27150 of 73748

  • SevereFDA (Food)·F-0057-2021·2020-10-28

    Sauer Brands Recalls Freeze-Dried Chives Due to Salmonella Risk

    Sauer Brands Inc is recalling The Spice Hunter Freeze-Dried Chives due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    The Spice Hunter Freeze-Dried Chives 0.13 oz. Jar UPC 8105701230 Case UPC 40081057012305
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0127-2021·2020-10-28

    GE Healthcare Recalls MRI Systems Due to Potential Electrical Arc Flash

    GE Healthcare is recalling 30 MRI systems due to a potential electrical arc flash hazard within the Power Gradient & RF cabinet.

    Product
    System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0088-2021·2020-10-28

    Medtronic Recalls Rashkind Balloon Septostomy Catheters Due to Field Failures

    Medtronic Vascular is recalling 711 units of Rashkind Balloon Septostomy Catheters due to subsequent field failures and failed quality testing.

    Product
    Rashkind Balloon Septostomy Catheter, 5F, Closed end, 50 cm, Pediatric, Single Lumen Product number: 007160 GTIN: 00613994760265 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial septal defect as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0046-2021·2020-10-28

    Sauer Brands Recalls Coriander Jars Due to Potential Salmonella Contamination

    Sauer Brands Inc is recalling The Spice Hunter Coriander jars due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Coriander 1.4 oz. Jar UPC 8105701275 Case UPC 40081057012756
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0255-2021·2020-10-28

    ICU Medical Recalls Intravascular Administration Sets Due to Manufacturing Defect

    ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect on the NanoClave may prevent a proper seal with the spike.

    Product
    148 IN (376cm) APPX 18.8 ml, 15 DROP SET, 2 CLAVE, Remv 3 Gang Clave Stopcock.1 unit per pouch, 25 pouches per case. UDI:(01)10887709071558(17)250101(30)25(10)4603841. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0222-2021·2020-10-28

    ICU Medical Recalls Intravascular Administration Sets Due to Seal Defect

    ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent a proper seal.

    Product
    123 IN (312cm) APPX 16.1 ml, 10 DROP SET w/3 MicroClave, 3-Port NanoClave; UDI:(01)10887709085432(17)241201(30)25(10)4536733;(01)10887709085432(17)250101(30)25(10)4573641. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0130-2021·2020-10-28

    GE Healthcare Recalls MRI Systems Due to Electrical Arc Flash Risk

    GE Healthcare is recalling 30 MRI systems worldwide due to a potential electrical arc flash hazard within the Power Gradient & RF Cabinet.

    Product
    System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0059-2021·2020-10-28

    Sauer Brands Recalls The Spice Hunter Cilantro Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling The Spice Hunter Cilantro jars due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Cilantro 0.3 oz. Jar UPC 8105701236 Case UPC 40081057012367
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0040-2021·2020-10-28

    Sauer Brands Recalls Saigon Organic Cinnamon Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling Saigon Organic Cinnamon jars due to potential Salmonella contamination. The product was sold nationwide and online.

    Product
    The Spice Hunter Saigon Organic Cinnamon 1.7 oz. Jar UPC 8105701245 Case UPC 40081057012459
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0048-2021·2020-10-28

    Sauer Brands Recalls Green Hatch Chile Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling specific jars of The Spice Hunter Green Hatch Chile due to potential Salmonella contamination. Consumers should check their pantries for the affected lot.

    Product
    The Spice Hunter Green Hatch Chile 2.4 oz. Jar UPC 8105702256 Case UPC 40081057022564
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0042-2021·2020-10-28

    Sauer Brands Recalls Sesame Seeds Due to Potential Salmonella Contamination

    Sauer Brands Inc is recalling The Spice Hunter Gourmet Sesame Seeds due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Gourmet Sesame Seeds 2.4 oz. Jar UPC 8105701937 Case UPC 40081057019373
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0055-2021·2020-10-28

    Sauer Brands Recalls Everything Bagel Crunch for Potential Salmonella

    Sauer Brands Inc is recalling The Spice Hunter Everything Bagel Crunch due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Everything Bagel Crunch 2.3 oz. Jar UPC 8105701351 Case UPC 40081057013517
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0049-2021·2020-10-28

    Sauer Brands Recalls Black Pepper Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling specific jars of The Spice Hunter Black Pepper and Fine Black Pepper due to potential Salmonella contamination.

    Product
    The Spice Hunter Black Pepper 1.7 oz. Jar UPC 8105701703 Case UPC 40081057017034, Fine Black Pepper 1.6 oz. Jar UPC 8105701706 Case UPC 40081057017065
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0258-2021·2020-10-28

    ICU Medical Recalls Burette Sets Due to Potential Manufacturing Defect

    ICU Medical is recalling specific lots of 112-inch burette sets because a manufacturing defect may prevent a proper seal with the NanoClave spike.

    Product
    112" (284 cm) 60 Drop 150ml Burette Set (Clave, Shut-Off) w/2 MicroClave, Remv 3 Gang 4-Way Clave Stopcock, Check Valve, Rotating Luer, 1 Ext. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709079127(17)250201(30)25(10)4727501. The Intravascular Administration Set is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0176-2021·2020-10-28

    Bien-Air Surgery Foot Pedal Recalled Due to Magnet Detachment Risk

    Bien-Air Surgery is recalling 1,120 foot pedals because an internal magnet may detach, causing the motor to start unattended and become unstoppable.

    Product
    Bien-Air Surgery REF 1600407-001 SN **** FOOTCTRL OSSEODOC - Product Usage: intended to convert electrical energy to mechanically drive handpieces and microsaws used to cut and shape bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0203-2021·2020-10-28

    ICU Medical Recalls Smallbore Intravascular Administration Sets Due to Seal Defect

    ICU Medical is recalling specific lots of smallbore intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.

    Product
    8.5" (22 cm) Appx 0.57 ml, Smallbore Ext Set w/NanoClave, 0.2 Micron Filter, Clamp, Rotating Luer;1 unit per pouch, 50 multivac pouches per case.UDI:(01)10887709077671(17)250101(30)50(10)4557524. The Intravascular Administration Set is a single use, sterile, non-pyrogenic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0043-2021·2020-10-28

    Sauer Brands Recalls Herbs De Provence Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling specific lots of The Spice Hunter Herbs De Provence due to potential Salmonella contamination.

    Product
    The Spice Hunter Herbs De Provence 0.6 oz. Jar UPC 8105701440 Case UPC 40081057014408
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0221-2021·2020-10-28

    ICU Medical Recalls NanoClave Intravascular Administration Sets Due to Seal Defect

    ICU Medical is recalling specific lots of NanoClave intravascular administration sets because a manufacturing defect may prevent a proper seal with the spike.

    Product
    83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way NanoClave¿ Stopcock w/Baseplate, Rotating Luer;1 unit per pouch, 25 pouches per case. UDI:(01)10887709089508(17)250101(30)25(10)4548244. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0186-2021·2020-10-28

    ICU Medical Recalls Smallbore Extension Sets Due to Seal Defect

    ICU Medical is recalling specific lots of 7-inch smallbore extension sets because a manufacturing defect may prevent the NanoClave from sealing properly.

    Product
    7" (18 cm) Appx 0.29 ml, Smallbore Ext Set w/MicroClave Clear, NanoClave, Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709051048(17)250101(30)50(10)4572718; (01)10887709051048(17)250101(30)50(10)4603246…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0246-2021·2020-10-28

    ICU Medical Recalls Intravascular Administration Sets Due to Manufacturing Defect

    ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.

    Product
    40 (102cm) Appx 4.4ml Ext Set, 4-Way Clave Stopcock, Clave, 2 Clamps, Rotating Luer, 1 Ext. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709014531(17)250101(30)50(10)4603496. The Intravascular Administration Set is a single use, sterile, non-pyrogenic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0193-2021·2020-10-28

    ICU Medical Recalls Smallbore Pressure Infusion Extension Sets

    ICU Medical is recalling specific lots of smallbore pressure infusion extension sets due to a potential manufacturing defect that may inhibit a proper seal.

    Product
    6.5" (17 cm) Appx 0.30 ml, Smallbore Pressure Infusion (400psig) Ext Set w/Remv MicroClave, NanoClave T-Connector, Purple Clamp, Rotating Luer. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709062525(17)250101(30)50(10)4558455…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0182-2021·2020-10-28

    ICU Medical Recalls NanoClave Connectors Due to Manufacturing Defect

    ICU Medical is recalling specific lots of NanoClave Connectors because a manufacturing defect may prevent a proper seal with the spike.

    Product
    NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051; (01)10887709051017(17)241101(30)100(10)4447754 CLAVE Neutron is a normally closed, bidirectional connector intended for use as an accessory to an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0172-2021·2020-10-28

    Smith & Nephew Recalls HEALICOIL Absorbable Suture Anchors Due to Seal Issues

    Smith & Nephew is recalling HEALICOIL absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.

    Product
    HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BLK- Absorbable Suture anchor Product Number: 72203708
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0259-2021·2020-10-28

    ICU Medical Recalls Smallbore Trifuse Extension Sets Due to Seal Defect

    ICU Medical is recalling specific lots of Smallbore Trifuse Extension Sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.

    Product
    5.5" (14 cm) Appx 0.39 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, NanoClave T-Connector, 3 Clamps, Rotating Luer.1 unit per pouch, 50 multivac pouches per case. UDI: (01)10887709032153(17)241101(30)50(10)4475297; (01)10887709032153(17)250201(30)50(10)4711598. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide