State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39726–39750 of 73919

HighFDA (Devices)·Z-0626-2018·2018-02-21
Zimmer Biomet Recalls G7 Dual Mobility Hip Liners Due to Labeling Error
Zimmer Biomet is recalling 8 units of G7 Dual Mobility Liners because they are labeled as 44mm but may physically be 42mm liners.
Product
G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to be replaced with artificial prosthesis. The result of the procedure is to relieve pain and restore a sense of normal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0625-2018·2018-02-21
Roche Recalls Accu-Chek Connect App Due to Bolus Advisor Software Bug
Roche Diabetes Care is recalling the Accu-Chek Connect app because a software bug may cause incorrect unit changes, risking inaccurate blood glucose data or carbohydrate input.
Product
Accu-Chek Connect Diabetes Management App, Catalog number 07562462001 / GTIN number 00365702700000 & Catalog number 07250452001 / GTIN number 00365702700017
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0591-2018·2018-02-21
Aesculap Vega Knee Trial Plateau Recalled for Incorrect Labeling
Aesculap is recalling 13 units of the NS357R Vega PS Tibia Trial/Preparation Plateau size T4 due to incorrect labeling. Using the wrong size could lead to implantation errors, ligament injury, pain, or revision surgery.
Product
NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of the Vega Knee System Set #ST0468) The affected part is provided in the Vega Knee System Set #ST0468. The Vega Knee System is used for reconstruction of the diseased knee joint.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0599-2018·2018-02-21
3M Bair Hugger Underbody Blanket Recall for Airflow Occlusion Risk
3M is recalling Bair Hugger Normothermia System blankets due to a design change that may cause unintended airflow occlusion and limited inflation.
Product
3M Bair Hugger(M) Normothermia System, Sterile Full Access Underbody, Model 63700 The 3M Bair Hugger Temperature Management System is intended to prevent and treat hypothermia. In addition, the temperature management system can be used to provide patient thermal comfort when…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18104·2018-02-21
Yayi Outdoor Gas Fire Pit Tables Recalled for Burn Hazard
Yayi is recalling Hampton Bay outdoor gas fire pit tables sold at Home Depot because the bowl base lacks a heat shield, posing a burn risk.
Product
Outdoor Gas Fire Pit Table Patio Heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0628-2018·2018-02-21
Zimmer Biomet Recalls AGC 2000 LP Patella Knee Implants
Zimmer Biomet is recalling 11 AGC 2000 LP Patella knee implants because they were over-molded, causing the outside diameter to not match the required specifications.
Product
AGC 2000 LP Patella, labeled as AGC Porous Patellar Med, Model Number 150804. Product Usage: For use in Total Knee Arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0627-2018·2018-02-21
Zimmer Biomet Recalls AGC 2000 LP Patella Knee Implant Devices
Zimmer Biomet is recalling 28 AGC 2000 LP Patella knee implants because they were over-molded, leaving the outside diameter nonconforming to the print dimension.
Product
AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee Arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0598-2018·2018-02-21
3M Bair Hugger Warming Blanket Recall for Airflow Occlusion Risk
3M is recalling Bair Hugger warming blankets because a design change may cause airflow blockage, leading to limited inflation during use.
Product
3M Bair Hugger(M) Normothermia System, Full Access Underbody Warming Blanket, REF 63500 The 3M Bair Hugger Temperature Management System is intended to prevent and treat hypothermia. In addition, the temperature management system can be used to provide patient thermal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0629-2018·2018-02-21
Hemotherm Dual Reservoir Cooler/Heater System Recall for Updated Cleaning Instructions
Cincinnati Sub-Zero is recalling 1,355 Hemotherm units to provide updated instructions for cleaning and disinfection to address NTM infection risks.
Product
Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR Product Usage: A dual reservoir, water re-circulating device that supplies temperature controlled water to a heat exchanger. The device, in conjunction with a heat exchanger, is used to warm or cool the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0396-2018·2018-02-21
Sage Products Recalls Q.CARE Oral Cleansing System Due to Cross-Contamination
Sage Products Inc is recalling Q.CARE Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q.CARE Oral Cleansing & Suctioning System q4. Contains 1 Covered Yankauer, Suction Handle and Y-Connector, 2 Toothbrush packages with Antiplaque solution. 4 Suction Oral Swab packages with Perox-A-Mint solution. 2 Oropharyngeal Suction Catheter packages, Sage Products, Inc.…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0351-2018·2018-02-21
Sage QCare Oral Cleansing System Recalled for Cross-Contamination Risk
Sage Products Inc. is recalling QCare Oral Cleansing and Suctioning Systems with Corinz due to cross-contamination with non-pharmaceutical products during manufacturing.
Product
QCare Oral Cleansing and Suctioning System with Corinz. Includes: Two (2) Suction Toothbrush packages with 0.25fl.oz/7mL Corinz Antiseptic Cleansing and Moisturizing Oral Rinse and Four (4) Suction Oral Swab packages with 0.25 fl.oz/7mL Corinze Antiseptic Cleansing and…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0601-2018·2018-02-21
Arrow International Recalls PICC Catheter Kits Due to Incorrect Components
Arrow International is recalling specific PICC catheter kits because they may contain the wrong catheter size or type, potentially delaying patient treatment.
Product
ARROW PICC powered by ARROW VPS Stylet, Product Codes: CDC-35052-VPS and CDC-35041-VPS. Peripherally Inserted Central Catheter
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0402-2018·2018-02-21
Sage Q.Care Oral Cleansing System Recalled for Cross-Contamination
Sage Products is recalling Q.Care Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q.Care Oral Cleansing & Suctioning System Suction Toothbrush Compatible with Chlorhexidine Gluconate (CHG) Oral Rinse q2. Contains 1 Covered Yankauer and Y-Connector, 2 Untreated, CHG Compatible Suction Toothbrush packages, 4 Suction Oral Swab packages with Perox-A-Mint…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0571-2018·2018-02-21
B. Braun Recalls Perifix FX Epidural Anesthesia Trays Due to Foreign Matter
B. Braun Medical is recalling Perifix FX Epidural Anesthesia Trays because they contain needles with loose polypropylene foreign matter above release specifications.
Product
Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993, 552051, 552083, 552119, 555569. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0630-2018·2018-02-21
Cook Inc. Recalls Central Venous Catheter Sets Due to Fit Issues
Cook Inc. is recalling 85 Central Venous Catheter Sets because they may not fit over a guide wire, potentially causing procedure delays.
Product
Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or intermittent drug infusions; 2. Central venous blood…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0415-2018·2018-02-21
Famciclovir Tablets Recalled Due to Temperature Abuse During Distribution
Hetero Labs Limited is recalling 8,436 bottles of Famciclovir 500 mg tablets because high temperatures during distribution caused the tablets to become wet, stuck together, and disintegrated.
Product
FAMCICLOVIR — FAMCICLOVIR (FAMCICLOVIR)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0371-2018·2018-02-21
Sage Products Recalls Q Care Oral Care Kits Due to Cross-Contamination
Sage Products Inc. is recalling Q Care Continue Care kits because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.
Product
Q Care Continue Care for the non-ventilated patient. Contains, 1 Covered Yankauer, 2 Suction Toothbrush packages with Corinz Antiseptic Cleansing and Moisturizing Oral Rinse, 2 Suction Oral Swab packages with Corinz Antiseptic Cleansing and Moisturizing Oral Rinse. Sage…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0618-2018·2018-02-21
Synthes USA Recalls Norian Drillable Inject Due to Expiration Date Mismatch
Synthes USA is recalling 5 units of Norian Drillable Inject because kit expiration dates do not align with the earliest component expiration dates.
Product
Norian Drillable Inject
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0359-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Systems Due to Cross-Contamination
Sage Products Inc. is recalling 835 cases of Toothette Oral Care Short Term Oral Swab Systems because they were manufactured on equipment shared with non-pharmaceutical products.
Product
Toothette Oral Care Short Term Oral Swab System with Perox-A- Mint solution. Contains 20 Toothette Plus Oral Swabs with sodium bicarbonate, 1.5 fl.oz/44ml bottle Perox-A-Mint solution, .5 oz/14g tube of Mouth Moisturizer, .3 oz./9g tube of Sodium Bicarbonate Mouthpaste, I…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0612-2018·2018-02-21
Zimmer Surgical Recalls A.T.S. 4000TS Tourniquet Systems for Labeling Updates
Zimmer Surgical Inc is recalling 8,231 A.T.S. 4000TS Tourniquet Systems to update on-device labels and operator manuals, and to reduce the required separation distance from RF communication equipment.
Product
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities. .
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0631-2018·2018-02-21
Cook Central Venous Catheter Tray Recalled for Fit Issues
Cook Inc. is recalling 25 Central Venous Catheter Trays because they may not fit over the guide wire, potentially causing procedure delays.
Product
Central Venous Catheter Tray Triple Lumen Polyurethane, Catalog Identifier: C-UTLMYJ-501J Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or intermittent drug infusions; 2. Central venous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0597-2018·2018-02-21
OrthoPediatrics Recalls 7.0mm Pedicle Screws Due to Color Anodizing Error
OrthoPediatrics Corp is recalling 24 units of 7.0mm x 40mm pedicle screws because they were color anodized with the same color used for 5mm screws.
Product
Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Usage: Posterior non-cervical pedicle screw fixation
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0569-2018·2018-02-21
B. Braun Recalls Pencan Spinal Needle Trays Due to Foreign Matter
B. Braun Medical is recalling 11,920 units of Pencan Spinal Needle Trays because they contain loose polypropylene foreign matter above release specifications.
Product
Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0570-2018·2018-02-21
B. Braun Recalls Perifix Epidural Anesthesia Trays Due to Foreign Matter
B. Braun Medical is recalling Perifix Epidural Anesthesia Trays because they contain needles with loose polypropylene foreign matter above release specifications.
Product
Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879, 551994, 552024. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0391-2018·2018-02-21
Sage Products Recalls Toothette Oral Care Suction Toothbrush
Sage Products is recalling Toothette Oral Care Suction Toothbrush kits due to cross-contamination with non-pharmaceutical products during manufacturing.
Product
Toothette Oral Care Suction Toothbrush with Perox-A-Mint solution. Contains 1 Suction Toothbrush with sodium bicarbonate, 0.25 fl oz/ 7ml Perox-A-Mint solution, 0.07 oz/2g Mouth Moisturizer, 1 Applicator Swab. Sage Products, Inc., 3909 Three Oaks Road, Cary, IL 60013. Product…
Category
Drug
Distribution
Distributed nationwide