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.

27101–27125 of 73748

  • CriticalFDA (Food)·F-0051-2021·2020-10-28

    Sauer Brands Recalls The Spice Hunter Paprika Due to Salmonella Risk

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

    Product
    The Spice Hunter Paprika 1.4 oz. Jar UPC 8105701653 Case UPC 40081057016532
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0035-2021·2020-10-28

    Acella Recalls NP Thyroid 15 Tablets Due to Subpotent Levothyroxine

    Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because FDA analysis found the levothyroxine content was less than the labeled claim.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0038-2021·2020-10-28

    Red Monkey Foods Recalls Herbes de Provence Due to Salmonella Risk

    Red Monkey Foods Inc is recalling specific packages of Herbes de Provence because an ingredient tested positive for Salmonella.

    Product
    Herbes de Provence packaged in the following ways: 1) World Market, Organic Herbs De Provence, Net Wt. 0.6 OZ (17 g), Distributed by Cost Plus, Inc., Alameda, CA UPC 2533 3107; 2) Organics, Herbs De Provence, Net Wt. 0.65 OZ (18 g), Distributed by Lucerne Foods, Inc.…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0037-2021·2020-10-28

    Red Monkey Foods Recalls Dried Parsley Due to Salmonella Contamination

    Red Monkey Foods Inc. is recalling 1,130 cases of dried parsley products because the ingredient tested positive for Salmonella. The products were distributed to retail stores nationwide.

    Product
    Dried Parsley packaged in the following ways: 1) World Market, Organic Parsley NET WT. 0.3 OZ (8.5 g), Distributed by Cost Plus, Inc., Alameda, CA UPC 2533 3251; 2) Organics, Organic Parsley, NET WT. 0.3 OZ (8.5 g), Distributed by Lucerne Foods, Inc., Pleasanton, CA UPC 0…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0131-2021·2020-10-28

    GE Healthcare Recalls PET/MR Imagers Due to Electrical Arc Flash Risk

    GE Healthcare is recalling specific PET/MR imager models due to a potential electrical arc flash hazard within the Power Gradient & RF Cabinet.

    Product
    Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance - Product Usage: The combined system maintains independent functionality of the MR and PET devices, allowing for single modality MR and / or PET imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0180-2021·2020-10-28

    Entellus Medical Shaver System Foot Pedal Recalled for Magnet Defect

    Bien-Air Surgery Sa is recalling Entellus Medical Shaver System foot pedals because an internal magnet may detach, causing the motor to start unattended and become unstoppable.

    Product
    Entellus Medical REF SSA-102 SN ******* Shaver System Foot Pedal - Product Usage: The Entellus Medical Shaver System has been designed for shaping bone and for the resection of soft and hard tissues as part of surgical procedures in the areas of otorhinolaryngology.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0044-2021·2020-10-28

    Sauer Brands Recalls Pumpkin Pie Spice Jars Due to Salmonella Risk

    Sauer Brands Inc is recalling 45,498 jars of The Spice Hunter Pumpkin Pie Spice due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Pumpkin Pie Spice 1.8 oz. Jar UPC 8105701850 Case UPC 40081057018505
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0054-2021·2020-10-28

    Sauer Brands Recalls Muntock White Pepper Due to Salmonella Risk

    Sauer Brands Inc is recalling Muntock White Pepper jars due to potential Salmonella contamination. The product was distributed nationwide and online.

    Product
    The Spice Hunter Muntock White Pepper 2.1 oz. Jar UPC 8105701792 Case UPC 40081057017928
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0061-2021·2020-10-28

    Sauer Brands Recalls Dill Weed Jars Due to Salmonella Risk

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

    Product
    The Spice Hunter Dill Weed 0.5 oz. Jar UPC 8105701348 Case UPC 40081057013487
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0230-2021·2020-10-28

    ICU Medical Recalls 114-inch Burette Sets Due to Seal Defect

    ICU Medical is recalling specific lots of 114-inch burette sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.

    Product
    114" (290 cm) 60 Drop 150ml Burette Set (Clave, Shut Off, Filter) w/4 Clave Remv 3-Port NanoClave Manifold, 2 Check Valves, Rotating Luer, 2 Exts. 1 unit per pouch, 25 pouches per case.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0177-2021·2020-10-28

    Bien-Air Surgery Multifunction Pedal Recalled Due to Magnet Failure Risk

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

    Product
    Bien-Air Surgery REF 1600517-001 SN ******* MULTIFUNCTION PEDAL OSSEODUO - Product Usage: Product Usage: intended to convert electrical energy to mechanically drive attachment, microsaws, shaver blades and burs, burs and perforator tools for cutting and shaping bone including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0052-2021·2020-10-28

    Sauer Brands Recalls Szechwan Seasoning Due to Salmonella Risk

    Sauer Brands Inc is recalling The Spice Hunter Szechwan Seasoning due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    The Spice Hunter Szechwan Seasoning 2.1 oz. Jar UPC 8105701955 Case UPC 40081057019557
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0179-2021·2020-10-28

    Stryker S2 Mini Foot Pedal Recalled Due to Magnet Defect

    Bien-Air Surgery is recalling Stryker S2 Mini Foot Pedals because an internal magnet may detach, causing the motor to start unattended and become unstoppable.

    Product
    Stryker Instruments REF 5452-007-000 SN ******* S2 MINI FOOT Pedal - Product Usage: The S2 Mini Drill System has been designed for the light drilling of bones as part of surgical operations such as stapedotomy or ossiculoplasty. The S2 Mini Drill System consists of a foot…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0089-2021·2020-10-28

    Medtronic Vascular Recalls Rashkind Balloon Septostomy Catheters Due to Field Failures

    Medtronic Vascular is recalling 505 units of Rashkind Balloon Septostomy Catheters due to subsequent field failures and failed quality testing.

    Product
    Rashkind Balloon Septostomy Catheter, 4F, Closed end, 50 cm, Pediatric, Single Lumen Product number: 007161 GTIN: 00613994760272 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 (Devices)·Z-0087-2021·2020-10-28

    Medtronic Rashkind Balloon Septostomy Catheter Recall for Quality Failures

    Medtronic Vascular is recalling Rashkind Balloon Septostomy Catheters due to field failures and failed quality testing. The recall covers 2,356 units distributed worldwide.

    Product
    Rashkind Balloon Septostomy Catheter, 6F, Recess Balloon, Closed end, 50 cm, Pediatric, Single Lumen Product number: 008764 GTIN: 00613994760289 The Rashkind balloon septostomy catheters are designed for creating an atrial septal defect or enlarging an existing atrial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0129-2021·2020-10-28

    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 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-0056-2021·2020-10-28

    Sauer Brands Recalls Malabar Black Peppercorns Due to Salmonella Risk

    Sauer Brands is recalling Malabar Black Peppercorns due to potential Salmonella contamination. Consumers should stop using the product and return it to the store of purchase.

    Product
    The Spice Hunter Malabar Black Peppercorns 2.1 oz. Jar UPC 8105701700 Case UPC 40081057017003
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0128-2021·2020-10-28

    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 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
  • SevereNHTSA·20V663000·2020-10-28

    Daimler Recalls 2015-2020 Sprinter Vans for Steering Hose Defect

    Daimler Vans USA is recalling 2015-2020 Mercedes-Benz and Freightliner Sprinter vans because hydraulic power steering hoses may detach, causing fluid leaks and loss of steering assist.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0118-2021·2020-10-28

    Smith & Nephew Recalls Genesis Knee Implants Due to Design Defect

    Smith & Nephew is recalling 47 Genesis knee implants because the anterior locking detail does not meet design specifications.

    Product
    Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are absent or incompetent.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0064-2021·2020-10-28

    Sauer Brands Recalls Holiday Spice Shipper Boxes Due to Salmonella Risk

    Sauer Brands Inc is recalling specific holiday spice shipper boxes nationwide and online due to potential Salmonella contamination.

    Product
    Shipper boxes - sent to retail stores for display. Spices contained in the boxes are currently under recall. Thanksgiving shipper - item # 43149 Holiday Gourmet Shipper - Item # 43142 Shipper - Organic Holiday - Item # 43143
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0119-2021·2020-10-28

    Olympus Choledoscope Recalled for Lack of Clearance and Breakage

    Olympus is recalling CHF-CB30S choledoscopes because they lack FDA clearance and have experienced breakage and metal protrusion during use.

    Product
    Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light source, TV monitor, endo-therapy accessories and other ancillary equipment for endoscopic diagnosis and treatment within the biliary tract (common bile…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0189-2021·2020-10-28

    ICU Medical Recalls Smallbore Bifuse Extension Sets Due to Seal Defect

    ICU Medical is recalling specific lots of 9-inch Smallbore Bifuse Extension Sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.

    Product
    9" (23 cm) Appx 0.63 ml, Smallbore Bifuse Ext Set w/2 MicroClave Clear, NanoClave, 3 Clamps, 0.2 Micron Filter, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case UDI:(01)10887709052953(17)241201(30)50(10)4536611;(01)10887709052953(17)250101(30)50(10)4557492 The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0050-2021·2020-10-28

    Sauer Brands Recalls Mexican Seasoning for Potential Salmonella Contamination

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

    Product
    The Spice Hunter Mexican Seasoning 1.4 oz. Jar UPC 8105701541 Case UPC 40081057015412
    Category
    Food
    Distribution
    Distributed nationwide