The Recall Desk

State

US Virgin Islands product recalls

73,737 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36001–36025 of 73915

  • ModerateFDA (Devices)·Z-0459-2019·2018-11-21

    Siemens Artis Q.zen Biplane X-Ray System Recalled for C-Arm Vibration

    Siemens Medical Solutions is recalling 15 Artis Q.zen biplane angiographic x-ray systems because C-arm vibrations may reduce image quality.

    Product
    ARTIS Q.zen biplane with Material 10848355 - a Angiographic x-ray system Product Usage: Artis zee is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0444-2019·2018-11-21

    Espiner Tissue Retrieval System Recalled for Incorrect Volume Labeling

    Espiner Medical Ltd is recalling 230 units of the Eco-Sac Tissue Retrieval System because the label incorrectly states the volume is 1200 ml instead of 1000 ml.

    Product
    Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml EMP160ECO-US-5 (GTIN:5060358120367) Product Usage: Tissue Retrieval sac made from ripstop nylon. The EMP160ECO-US-5 is a semi-automatic sac, which incorporates a monofilament drawstring around the mouth of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0455-2019·2018-11-21

    Straumann Recalls Neodent GM Mini Conical Abutments Due to Label Mismatch

    Straumann Manufacturing is recalling 21 units of Neodent GM Mini Conical Abutments because the laser-engraved label does not match the item in the package.

    Product
    Neodent¿ GM Mini Conical Abutment - Product Usage: Mini Conical Abutments are intermediary prosthetic components to be installed onto GM implants to support the final prosthesis. They are provided in a rotational shape for the coupling with the prosthesis and in different…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0446-2019·2018-11-21

    BioFire FilmArray Meningitis/Encephalitis Panel Recalled for False Positive Risk

    BioFire Diagnostics is recalling specific FilmArray Meningitis/Encephalitis (ME) Panel kits due to a manufacturing issue that may cause elevated rates of false positive results for HSV-1.

    Product
    -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME) Panel REF RFIT-ASY-0118 30 For FilmArray systems LOT KIT UDI (01)00815381020123 CE 0086 IVD -Fitment Label (P/N RFIT-LBL-0138) which identifies the pouch label - FilmArray¿ ME Panel v1.4…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0277-2019·2018-11-21

    Taro Recalls Children's Allergy Oral Solution Due to Impurity

    Taro Pharmaceuticals is recalling 8,328 bottles of Children's Allergy (cetirizine hydrochloride) oral solution because an unknown impurity exceeded specified limits during stability testing.

    Product
    CHILDRENS ALLERGY — CHILDRENS ALLERGY (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0458-2019·2018-11-21

    Siemens ARTIS Q Biplane Recalled for C-Arm Vibration Issues

    Siemens is recalling 54 ARTIS Q biplane x-ray systems because C-arm vibrations may reduce image quality due to a ceiling support screw connection.

    Product
    ARTIS Q biplane with Material 10848282- - a Angiographic x-ray system Product Usage: Artis zee is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0257-2019·2018-11-21

    Sandoz Recalls Nitrofurantoin Capsules Due to Cross Contamination

    Sandoz Inc is recalling specific lots of Nitrofurantoin capsules because they may be cross-contaminated with other products.

    Product
    NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS) — NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS) (NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS))
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0279-2019·2018-11-21

    Breckenridge Recalls Megestrol Acetate Oral Suspension for Stability Failures

    Breckenridge Pharmaceutical is recalling Megestrol Acetate Oral Suspension due to out-of-specification particle size results during stability testing.

    Product
    Megestrol Acetate Oral Suspension, USP 625 mg/5mL, 150 mL bottle, Rx only, Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487, Manufactured by: Pharmaceutics International Inc. Hunt Valley, MD 21031
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0262-2019·2018-11-21

    Sandoz Recalls Nitrofurantoin Capsules Due to Cross-Contamination

    Sandoz Inc. is recalling specific lots of Nitrofurantoin Capsules 100 mg due to cross-contamination with other products.

    Product
    Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, 100-count bottoles, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141 Manufactured by: Sandoz Inc. Princeton, NJ 08540,NDC 16714-439-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V823000·2018-11-20

    Grand Design Recalls 2019 Imagine Trailers Due to Bearing Defect

    Grand Design is recalling 2019 Imagine recreational trailers because inner hub bearings may overheat and fail, increasing crash risk.

    Product
    GRAND DESIGN — GRAND DESIGN IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·116-2018·2018-11-20

    Long Phung Recalls Pork Products Due to Possible Listeria Contamination

    Long Phung Food Products is recalling ready-to-eat pork products due to possible Listeria monocytogenes contamination linked to four confirmed illnesses.

    Product
    165368 C. Corporation — 165368 C. Corporation Recalls Pork Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V819000·2018-11-20

    Heartland Recalls 2019 Trailers Due to Bearing Grease Defect

    Heartland is recalling 2019 Pioneer and Prowler trailers because inner hub bearings may overheat and fail, increasing crash risk.

    Product
    HEARTLAND — HEARTLAND PIONEER, PROWLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V821000·2018-11-20

    Navistar Recalls 2019-2020 IC Bus CE School Buses for Brake Line Defect

    Navistar is recalling 187 IC Bus CE school buses from 2019-2020 because an improperly routed brake air line may kink, causing the vehicle to pull right or disabling anti-lock brakes.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19036·2018-11-20

    Seabreeze Recalls Smart Thermaflo Bathroom Heater Fans Due to Fire Hazard

    Seabreeze International is recalling Smart Thermaflo Bathroom Heater Fans because the safety cutoff can fail, allowing the unit to overheat and catch fire.

    Product
    Smart Thermaflo Bathroom Heater Fans with nightlight
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V822000·2018-11-20

    RAM Recalls 2019 1500 Trucks for Passenger Seat Sensor Defect

    Chrysler is recalling 2019 RAM 1500 trucks because a loose passenger seat sensor may prevent proper airbag deployment, increasing injury risk in a crash.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V820000·2018-11-20

    Cruiser RV Recalls 2019 MPG and Radiance Ultra Lite Trailers

    Cruiser RV is recalling 2019 MPG and Radiance Ultra Lite trailers because inner hub bearings may overheat and fail, increasing crash risk.

    Product
    CRUISER RV — CRUISER RV RADIANCE ULTRA LITE, MPG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19718·2018-11-20

    HoMedics Recalls Giraffe Nightlights Due to Choking Hazard

    HoMedics is recalling MyBaby Giraffe Nightlights because small feet can detach, posing a choking hazard to small children.

    Product
    MyBaby Giraffe Nightlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V818000·2018-11-19

    Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Repair

    Volkswagen Group of America is recalling 2007-2012 Audi Q7 and 2009-2012 Audi Q5 vehicles to replace fuel pump flanges and install butyl tape to prevent fuel leaks and fire risk.

    Product
    AUDI — AUDI Q5, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18T016000·2018-11-19

    Yokohama Recalls RY023 Tires Due to Tread Separation Risk

    Yokohama is recalling specific RY023 tires because the rubber compound may be incorrect, potentially causing the tread to separate from the casing and increasing the risk of a crash.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V815000·2018-11-16

    Autocar Recalls 2019 Xpeditor Vehicles Due to Steering Bracket Defect

    Autocar is recalling 761 2019 Xpeditor vehicles because the power steering assist cylinder bracket may not be properly secured, potentially causing a loss of steering ability.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V813000·2018-11-16

    ARBOC Transit Bus Recall for Foldaway Seat Locking Defect

    ARBOC is recalling 2015-2018 Spirit of Freedom, Mobility, and Independence buses because foldaway seat cushions may not stay locked during a crash.

    Product
    ARBOC — ARBOC, ARBOC SPECIALTY VEHICLES SPIRIT OF INDEPENDENCE, SPIRIT OF MOBILITY, SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E105000·2018-11-16

    IMT Omnex Wireless Transmitters Recalled for Unintended Crane Movement

    Iowa Mold Tooling Co. is recalling Omnex Proportional Wireless Transmitters because a failing diode may cause cranes to move unexpectedly, increasing injury risk.

    Product
    ELECTRICAL SYSTEM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V812000·2018-11-16

    Thor Motor Coach Recalls 2017-2019 Motorhomes for Windshield Shade Defect

    Thor Motor Coach is recalling 2017-2019 Challenger, Miramar, and Outlaw motorhomes because the driver's windshield roller shade may unroll unexpectedly, blocking visibility.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OUTLAW, CHALLENGER, MIRAMAR
    Category
    Vehicle
    Distribution
    Distributed nationwide