State

US Virgin Islands product recalls

73,106 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: 30
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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12876–12900 of 73283

SevereFDA (Drugs)·D-0240-2024·2024-01-24
Old Spice Sweat Defense Spray Recalled for Benzene Contamination Nationwide
Old Spice Sweat Defense Pure Sport Plus anti-perspirant spray is being recalled nationwide due to benzene contamination in specific lot numbers. Consumers should discontinue use of affected products immediately.
Product
Old Spice, SWEAT DEFENSE PURE SPORT PLUS, Dry Spray, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT 3.8 oz (107 g) cans, Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-387-10, UPC 0 37000 72974 7
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0709-2024·2024-01-24
Express Chest Drains Recalled for Infection Risk from Recalled Syringes
Maquet Cardiovascular is recalling Express chest drains pre-packaged with recalled sterile water syringes. If not kept upright, patients may be exposed to infectious material, risking infection, abscess, sepsis, and death.
Product
Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0242-2024·2024-01-24
Secret Powder Fresh Antiperspirant Spray Recalled for Benzene Contamination
The Procter & Gamble Company is recalling Secret antiperspirant/deodorant spray due to the presence of benzene, a chemical contaminant. The recall affects multiple lot numbers distributed nationwide and internationally.
Product
SECRET ANTIPERSPIRANT — SECRET ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0710-2024·2024-01-24
FDA Recalls Express Chest Drain Blood Recovery Units Over Infection Risk
Maquet Cardiovascular is recalling Express chest drain units with defective sterile water syringes. If not kept upright, patients risk exposure to infectious material that may cause infection, abscess, sepsis, or death.
Product
Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0233-2024·2024-01-24
Sodium Bicarbonate Injection recalled for glass particulate contamination
Pfizer is recalling 34,000 cartons of 4.2% Sodium Bicarbonate Injection nationwide due to glass particles in the solution. Patients should immediately stop use and contact their supplier.
Product
4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0244-2024·2024-01-24
Secret Dry Spray Antiperspirant Recalled Due to Benzene Contamination
Procter & Gamble is recalling Secret Dry Spray Antiperspirant due to benzene contamination in specific lot numbers. The FDA has classified this as a Class I recall.
Product
Secret, Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0234-2024·2024-01-24
FDA Recalls Sodium Bicarbonate Injection Due to Glass Particle Contamination
Pfizer Inc. is recalling 21,200 cartons of Sodium Bicarbonate Injection (lot HA7295, expiring March 1, 2025) nationwide due to glass particle contamination. The product is distributed in the United States and Puerto Rico.
Product
SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0235-2024·2024-01-24
Atropine Sulfate Injection Recalled for Glass Particulate Matter Contamination
Pfizer Inc. is recalling Atropine Sulfate Injection due to glass particulate matter contamination in lot GY2496. This FDA Class I recall affects 24,400 cartons distributed nationwide in the USA and Puerto Rico.
Product
ATROPINE SULFATE — ATROPINE SULFATE (ATROPINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0243-2024·2024-01-24
Secret Dry Spray Antiperspirant recalled due to benzene contamination
The FDA has recalled Secret Dry Spray Antiperspirant due to benzene contamination in certain lots. Affected products were distributed nationwide in the USA, Puerto Rico, Canada, and internationally.
Product
Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Waterlily, Topical Spray Can, Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-381-10; UPC 0 37000 72372 1; 12/pack UPC 0 37000 72991 4
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0238-2024·2024-01-24
Old Spice PURE SPORT Anti-Perspirant Spray Recalled for Benzene Contamination
Old Spice PURE SPORT Anti-Perspirant Spray is recalled for benzene contamination in certain lot numbers. The product was distributed nationwide and internationally.
Product
Old Spice, PURE SPORT, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant & Deodorant Spray, Topical spray can, Net WT 6.0 OZ (170g), Distributed by Procter & Gamble, Cincinnati, OH 45202. NDC: 37000-199-60, UPC 0 12044 00191 2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0236-2024·2024-01-24
Topical Drug Recalled: Americaine Benzocaine Spray Contaminated with Benzene
Americaine benzocaine 20% topical anesthetic spray is being recalled nationwide due to benzene chemical contamination. The recall affects 34,704 cans with lot number 1A16420 and expiration date 01/31/2025.
Product
AMERICAINE — AMERICAINE (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0246-2024·2024-01-24
Secret Dry Spray Antiperspirant Recalled for Benzene Contamination
The FDA is recalling Secret Dry Spray antiperspirant (Lot #12001458SF) due to benzene contamination. Consumers should stop using the product immediately.
Product
Secret, Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Rose, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-380-10, UPC 0 37000 79884 2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0809-2024·2024-01-24
Enfamil Nutramigen Infant Formula Recalled for Potential Cronobacter Contamination
Mead Johnson is recalling Enfamil Nutramigen Hypoallergenic Infant Formula Powder due to potential Cronobacter sakazakii contamination. Approximately 1.4 million cans with specific UPC codes (300871239418 or 300871239456) and January 1, 2025 use-by date are affected.
Product
Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ and 19.8 OZ). UPC Code of 300871239418 or 300871239456 and Use By Date of "1 Jan 2025".
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0241-2024·2024-01-24
Old Spice Anti-Perspirant Spray Recalled Due to Benzene Contamination
Old Spice Sweat Defense Ultimate Captain anti-perspirant spray is being recalled due to benzene contamination. The FDA Class I recall affects products distributed nationwide and internationally.
Product
Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum Chlorohydrate 23.5%, Anti-Perspirant, Topical spray can 3.8 OZ (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-385-10, UPC 0 37000 74947 9
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0248-2024·2024-01-24
Secret OUTLAST Dry Spray Antiperspirant Recalled for Benzene Contamination
Procter & Gamble is recalling Secret OUTLAST Dry Spray antiperspirant (3.8 oz) due to potential benzene contamination at the manufacturing facility. All lots expiring through September 2023 are affected.
Product
Secret OUTLAST Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Protecting Powder, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-478-10, UPC 0 37000 74772 7
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0758-2024·2024-01-24
Maquet Volista OR Light Systems Recalled for Fall Hazard
Getinge is recalling Maquet Volista OR light systems that may fall during use in operating rooms. Approximately 236,793 units are affected nationwide and globally.
Product
Maquet Volista, Volista Access, Volista Access II, Volista Standop OR Light System, Model Numbers and Catalog Numbers ROL B FOR VLT400SF STP - ARDROL309001A, ROL B FOR VLT400SF STP - ARDROL309001C, ROL B FOR VLT600SF STP - ARDROL309003A, ROL B FOR VLT600SF STP - ARDROL309003C…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0743-2024·2024-01-24
High Pressure Rotator Infusion Device Recalled Due to Seal Defect
Smiths Medical is recalling 31,685 HIGH PRESSURE ROTATOR infusion devices with a manufacturing defect that may cause an inadequate seal. The defect could lead to medication leaks and under-infusion.
Product
HIGH PRESSURE ROTATOR WITH MALE LUER LOCK, List Number MX496HP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0744-2024·2024-01-24
High Pressure Rotator with O-Ring Seal Defect Recalled Worldwide
Smiths Medical is recalling High Pressure Rotators due to a manufacturing defect affecting O-ring seals. An oversized inner diameter may cause inadequate seal integrity, risking medication under-infusion.
Product
HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0753-2024·2024-01-24
Calibration Serum with Mis-assigned Alkaline Phosphatase Target
Randox Calibration Serum Level 3 has an incorrect Alkaline Phosphatase target value (approximately 10% off) affecting clinical chemistry testing on RX Series instruments.
Product
Calibration Serum Level 3 - IVD For use as a Calibrator in clinical chemistry assays Catalog Number: CAL2351
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0732-2024·2024-01-24
CareEvent Medical Device Push Notifications May Fail to Send
The CareEvent patient monitoring device may fail to send push notifications, potentially delaying detection of patient condition changes.
Product
(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0720-2024·2024-01-24
Field Cricothyrotomy Kit Recalled for Incompatible Endotracheal Tube Holder
Sarnova HC is recalling the Curaplex Field Cric Kit due to an incompatible endotracheal tube holder that prevents practitioners from securing the tube during cricothyrotomy procedures. The recall affects 1,063 kits distributed nationwide.
Product
Curaplex Field Cric Kit with ET Tube, Item Number 36611. The kit provides healthcare professionals with an assortment of supplies to perform a cricothyrotomy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0239-2024·2024-01-24
Old Spice Anti-Perspirant Spray Recalled Due to Facility Benzene Contamination
Old Spice SWEAT DEFENSE Dry Spray anti-perspirant is being recalled due to manufacturing facility issues where other product lots were found contaminated with benzene. No illnesses have been reported.
Product
Old Spice, SWEAT DEFENSE, STRONGER SWAGGER, Dry Spray, 48 Hour, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical Spray Can, Net WT 3.8 oz (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC 69423-386-10, UPC 0 37000 73034 7 OR UPC 0 12044 04475 9 (12 Pack…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0721-2024·2024-01-24
Curaplex Cricothyrotomy Field Kit Recalled for Incompatible Tube Holder
Sarnova HC recalls 15 Curaplex Cricothyrotomy Field Kits nationwide due to an incompatible endotracheal tube holder that prevents proper tube securement during cricothyrotomy procedures.
Product
Curaplex Cricothyrotomy Field Kit with Instruments, Kwik Cric MVP, 6.0mm, Item Number 351631i-A. The kit provides healthcare professionals with an assortment of supplies to perform a cricothyrotomy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0751-2024·2024-01-24
Medical Device Calibration Serums Recalled Due to Instructional Transcription Errors
Randox Laboratories has recalled multiple calibration serum products due to transcription errors in the Instructions for Use, which contain incorrect target values for several analytes.
Product
Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assayed Multi-Sera Level 3 (HE 1532)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0247-2024·2024-01-24
Secret OUTLAST Dry Spray Antiperspirant recalled for potential benzene contamination
Procter & Gamble is recalling Secret OUTLAST Dry Spray Antiperspirant due to a manufacturing facility deviation where other lots were found contaminated with benzene. The recalled product was manufactured at the affected facility.
Product
Secret, OUTLAST, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Completely Clean, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-384-10, UPC 0 37000 74764 2
Category
Drug
Distribution
Distributed nationwide