The Recall Desk

State

US Virgin Islands product recalls

73,388 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
39
Most recent
2026-09-23

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22376–22400 of 73565

  • SevereFDA (Drugs)·D-0280-2022·2021-12-22

    Lidocaine Topical Solution Recalled for Superpotency

    Teligent Pharma, Inc. is recalling Lidocaine Hydrochloride Topical Solution USP 4% nationwide due to the drug being superpotent. Affected lots are 13262 (Exp. 03/2022) and 14217 (Exp. 08/2022).

    Product
    Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL glass bottles, Rx Only, Teligent Pharma Inc., Buena, NJ 08310, NDC 52565-009-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0337-2022·2021-12-22

    FDA Class I Recall: Cardiosave Rescue Intra-Aortic Balloon Pump Fluid Ingress

    Datascope is recalling Cardiosave Rescue Intra-Aortic Balloon Pump devices due to possibility of fluid ingress, which could short electronic components and cause unsafe system shutdown.

    Product
    Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75, 0998-UC-0800-75, 0998-00-0800-83, 0998-UC-0800-83, 0998-00-0800-85, 0998-UC-0800-85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·22034·2021-12-22

    Hang-on Treestands Recalled Due to Cable Failure and Fall Hazard

    Big Game Treestands' 2021 The Captain model (batch 2M-0121) is recalled because plastic-coated cable crimps can slip during use, releasing the standing platform and causing falls. Two injuries have been reported from ten documented incidents.

    Product
    The Captain Hang-on Treestands (2021 Batch #2M-0121)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0336-2022·2021-12-22

    Cardiosave Hybrid IntraAortic Balloon Pump Recall Due to Fluid Ingress Risk

    Datascope Corp. is recalling Cardiosave Hybrid IntraAortic Balloon Pumps due to the risk of fluid entering the device, which could cause system failure and hemodynamic instability.

    Product
    Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-UC-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-UC-0800-34, 0998-00-0800-35, 0998-UC-0800-35, 0998-00-0800-36, 0998-UC-0800-36, 0998-00-0800-45…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0375-2022·2021-12-22

    Cardinal Health Recalls RoyalSilk Surgical Gowns for Compromised Packaging Seals

    Cardinal Health is recalling 364,481 units of RoyalSilk Non-Reinforced Surgical Gowns due to potential for open packaging seals that could compromise sterility. The recalled units were distributed worldwide.

    Product
    RoyalSilk Non-Reinforced Surgical Gowns Large SKU: 9518
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0328-2022·2021-12-22

    Kool-Aid Ice Blue Raspberry Lemonade Drink Mix Recalled for Glass and Metal

    Kraft Heinz Foods Company is recalling Kool-Aid ice blue raspberry lemonade drink mix powder (20 oz.) due to potential glass and metal contamination in the product.

    Product
    Kool-Aid ice blue raspberry lemonade drink mix powder 20 oz. UPC 043000954072
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0365-2022·2021-12-22

    Orthopedic Femur Plate Recalled for Incorrect MRI Safety Information

    Smith & Nephew is recalling 35 units of EVOS Condylar Medial Distal Femur Plate due to incorrect MRI scanning safety information in the product instructions. The instructions contained erroneous data that could affect patient safety during MRI procedures.

    Product
    smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, L, 5H, 115MM, REF 72573102
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0361-2022·2021-12-22

    Medline Venous Access Pack-LF Recalled for Expired Saline Component

    Medline is recalling Venous Access Pack-LF Convenience Kits because the included saline solution component expired before the kit's labeled expiration date, creating a quality and safety issue.

    Product
    Venous Access Pack-LF Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0330-2022·2021-12-22

    Kool-Aid Tropical Punch Drink Mix Recalled for Glass and Metal Contamination

    Kraft Heinz Foods is recalling Kool-Aid Tropical Punch "on the go" 10-pack drink mix powder due to potential contamination with glass and metal fragments. The affected product was distributed nationwide and internationally.

    Product
    Kool-Aid Tropical Punch "on the go" 10 pack net wt. 6.6 oz. drink mix powder UPC 043000023464
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0371-2022·2021-12-22

    Surgical gowns recalled due to potential compromised sterility from packaging seals

    Cardinal Health is recalling 363,480 units of SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns due to potential open packaging seals that could compromise product sterility.

    Product
    SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns X-large, X-long SKU: 9041EL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0381-2022·2021-12-22

    Boston Scientific ROTAPRO System Console Recalled for Manufacturing Instruction Deficiency

    Boston Scientific recalled 7 ROTAPRO rotational atherectomy system consoles due to incomplete manufacturing instructions regarding proper handling of the pneumatic kit component upon failure. Affected devices were distributed in six US states and Germany.

    Product
    Boston Scientific ROTAPRO, Rotational Atherectomy System Console, Model numbers H74939309010 (US) and H74939309030 (EU).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0325-2022·2021-12-22

    Country Time Half Lemonade and Half Iced Tea Drink Mix Recalled for Glass and Metal

    Kraft Heinz Foods Company is recalling Country Time Half lemonade and Half iced tea drink mix powder due to potential glass and metal fragments in the product.

    Product
    Country Time Half lemonade and Half iced tea drink mix powder 19 oz. UPC 043000046005 82.5 oz. UPC 043000046012
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0379-2022·2021-12-22

    Olympus EVIS EXERA II Duodenovideoscope Recalled for Contamination Risk

    Olympus TJF-Q180V duodenovideoscopes with adhesive deterioration or damage may pose infection risk due to endoscope contamination. Approximately 14,447 units are affected.

    Product
    EVIS EXERA II DUODENOVIDEOSCOPE OLYMPUS TJF-Q180V Model Number: TJF-Q180V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0321-2022·2021-12-22

    Country Time Pink Lemonade Powder Recalled for Glass and Metal Contamination

    Kraft Heinz Foods Company is recalling Country Time Pink Lemonade powder drink mix in 19 oz., 63 oz., and 82.5 oz. packages due to potential glass and metal contamination.

    Product
    Country Time Pink Lemonade powder drink mix 19 oz. UPC 043000951149 63 oz. UPC 043000082188 82.5 oz. UPC 043000928615
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0324-2022·2021-12-22

    Country Time "On The Go" Lemonade Drink Mix Powder Recall

    Kraft Heinz Foods Company is recalling Country Time "On The Go" Lemonade 10-pack drink mix powder due to potential glass and metal contamination in the product.

    Product
    Country Time "on the go" Lemonade 10 pack net wt. 6.7 oz. drink mix powder UPC 043000010983
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0372-2022·2021-12-22

    Cardinal Health Surgical Gowns Recalled for Potential Sterility Compromise

    Cardinal Health is recalling approximately 17,174 Poly-Reinforced Surgical Gowns (Large, SKU 9010) due to potential compromise of packaging seals that could affect product sterility. Units were distributed worldwide.

    Product
    Cardinal Health Poly-Reinforced Surgical Gowns Large SKU: 9010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0368-2022·2021-12-22

    SmartGown Breathable Surgical Gowns recalled for packaging seal defects

    Cardinal Health is recalling SmartGown Breathable Surgical Gowns because packaging seals may not remain intact, potentially compromising the gowns' sterility. The recall affects 224,312 units distributed in the US and internationally.

    Product
    SmartGown Breathable Surgical Gowns with raglan sleeves X-large, X-long, A-line SKU: 32474
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22038·2021-12-22

    Pearl River Propane Hoses Recalled for Fire Hazard Risk

    Pearl River propane hoses used with Flame King torches can swell and rupture, leaking propane gas and creating a fire hazard. About 43,000 units sold online from January through May 2021 are affected.

    Product
    Pearl River propane hoses used on propane torches and accessories
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0378-2022·2021-12-22

    Cardinal Health RoyalSilk Surgical Gowns Recalled for Sterility Compromise

    Cardinal Health is recalling 8,950 units of RoyalSilk Non-Reinforced Surgical Gowns due to potential packaging seal defects that could compromise sterility. The affected gowns were distributed worldwide.

    Product
    RoyalSilk Non-Reinforced Surgical Gowns XXX-large, X-long SKU: 95998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0359-2022·2021-12-22

    Neuro Convenience Kit recalled due to expired injectable component

    Medline Industries is recalling the Neuro Convenience Kit because a NaCl injectable component expired in April 2020 while the kit's overall expiration date was later. The expired component may pose a safety risk.

    Product
    Neuro Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0333-2022·2021-12-22

    Tang Guava Pineapple Drink Mix Powder Recalled for Glass and Metal

    Kraft Heinz Foods Company is recalling Tang guava pineapple drink mix powder (18 oz.) due to potential glass and metal fragments in the product. Affected packages have a Best When Used By date of 8/13/2023.

    Product
    Tang guava pineapple drink mix powder 18 oz. UPC 043000064511
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0373-2022·2021-12-22

    Cardinal Health Surgical Gowns X-Large Recalled for Packaging Seal Defect

    Cardinal Health is recalling 146,939 units of Poly-Reinforced Surgical Gowns (X-large, SKU 9040) due to potential compromised packaging seals that could affect sterility. Affected products were distributed worldwide.

    Product
    Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0366-2022·2021-12-22

    Smith & Nephew EVOS Condylar Plate Recalled for Incorrect MRI Instructions

    Smith & Nephew is recalling 41 units of the EVOS Condylar Medial Distal Femur Plate due to erroneous MRI scanning conditions in the instructions for use.

    Product
    smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE, R, 5H, 115MM, REF 72573202
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0363-2022·2021-12-22

    Smith & Nephew EVOS femur plates recalled for erroneous MRI instructions

    Smith & Nephew is recalling 38 EVOS femur plates because the product instructions contain erroneous MRI scanning conditions. The affected units were distributed nationwide across 14 states.

    Product
    smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE, L, 5H, 90MM, REF 72573101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00G000·2021-12-22

    Alamo Recalls 2012-2021 Schwarze CNG Street Sweepers for Fire Risk

    Alamo Group is recalling 2012-2021 Schwarze A7, A8, and A9 CNG street sweepers because debris accumulation against the exhaust system increases the risk of a fire.

    Product
    SCHWARZE — SCHWARZE A7 CNG STREET SWEEPER, A8 CNG STREET SWEEPER, A9 CNG STREET SWEEPER
    Category
    Vehicle
    Distribution
    Distributed nationwide