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.

Which agencies issued them

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.

20901–20925 of 73565

HighFDA (Devices)·Z-1008-2022·2022-05-04
Diabetes Management Software May Display Wrong Patient Data
Roche Diabetes Care Platform Software version 2.5.2 may display incorrect patient data when users navigate between patient records using the browser back button. No illnesses have been reported.
Product
RocheDiabetes Care Platform Software version 2.5.2 material number 08888353001. This is a web application software hosted on a server. There is no physical product.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0995-2022·2022-05-04
CT Scanner Software Update May Display Incorrect Laser Offset Coordinates
Siemens CT scanner software upgrade may cause incorrect laser offset coordinates to display during patient positioning. No injuries reported.
Product
syngo.via RT Image Suite upgraded to VB60 running on SOMATOM go.Up Model Number 11061620. Running on servers with syngo.via VB60 software after upgrade and CT scanners with syngo.CT VA40A after upgrade.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0813-2022·2022-05-04
Compounded Injectable Drug Recalled Due to Manufacturing Process Violations
Olympia Compounding Pharmacy is recalling 1,849 vials of RE-1, a compounded injectable medication, due to CGMP deviations in environmental and personnel monitoring. Monitoring excursions were not properly investigated prior to October 2021.
Product
RE-1, Papaverine 30 mg/mL . Phentolamine 3 mg/mL . Alprostadil 200 mcg/mL, Packaged in a) 10 mL Multi-Dose vial, NDC 73198-0015-10; b) 2.5 mL Multi-Dose vial, NDC 73198-0015-03; Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0805-2022·2022-05-04
Compounded injectable drug recall due to manufacturing quality control deviations
Olympia Compounding Pharmacy is recalling T-101, an injectable medication distributed nationwide, due to manufacturing quality control deviations in environmental and personnel monitoring prior to October 2021.
Product
T-101, Papaverine 17.65 mg/mL . Phentolamine 0.59 mg/mL . Alprostadil 5.9 mcg/mL. Packaged as a) 10 mL Multi-Dose vial, NDC 73198-0014-10; b) 5 mL Multi-Dose vial, NDC 73198-0014-05; Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0991-2022·2022-05-04
PrisMax Dialysis System Software Bug Silently Reverts Patient Treatment Parameters
The PrisMax dialysis system has a software bug that silently reverts treatment parameters to default values without notifying operators, affecting 1,253 units worldwide.
Product
PrisMax System, Product Code 955626
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1011-2022·2022-05-04
Smart Toe II Surgical Implant Recalled: Obscured Nickel Warning Label
Stryker GmbH recalls 246 Smart Toe II orthopedic implants due to label obstruction that obscures the nickel-sensitivity contraindication, potentially allowing inappropriate use.
Product
Smart Toe II Intramedullary Arthrodesis Implant
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0819-2022·2022-05-04
Alprostadil Injection Recalled Over Manufacturing Quality Control Failures
Olympia Compounding Pharmacy recalled PGE-3 Alprostadil 150 mcg/mL injection due to manufacturing facility failure to properly investigate environmental and personnel monitoring excursions.
Product
PGE-3, Alprostadil 150 mcg/mL, 10ml Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0030-10.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0211-2024·2022-05-04
Suave Aerosol Antiperspirant Recalled for Potential Benzene Contamination
Unilever is recalling all lots of Suave 24-Hour Protection Aerosol Antiperspirant Fresh scent nationwide due to potential benzene contamination at the manufacturing facility.
Product
Suave 24-Hour Protection Aerosol Antiperspirant Fresh scent, Aluminum Chlorohydrate (19.1%), packaged in 6 oz. cans, Unilever, Dist. By Unilever, Trumbull, CT 06611 UPC 0 79400 78550 3
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0993-2022·2022-05-04
PrisMax System software anomaly affects therapy parameter settings
The PrisMax System has a software defect that can silently revert custom therapy parameters to defaults when using the Same Patient function without notifying the operator.
Product
PrisMax System, Product Codes: a) 955558, b) 955627, c) 955701
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0996-2022·2022-05-04
CT scanner software upgrade causes incorrect laser position display
Siemens CT scanner software upgrade may display incorrect laser offset coordinates during patient marking. This defect affects 15 systems in the US across multiple states.
Product
syngo.via RT Image Suite upgraded to VB60 running on SOMATOM go.Sim Model Number 11061660. Running on servers with syngo.via VB60 software after upgrade and CT scanners with syngo.CT VA40A after upgrade.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0822-2022·2022-05-04
Phenylephrine Injectable Recalled Due to Manufacturing Quality Control Deviations
Olympia Compounding Pharmacy is recalling 4,521 vials of Phenylephrine 1 mg/mL due to manufacturing quality control failures. Environmental and personnel monitoring procedures were not properly investigated prior to October 1, 2021.
Product
Phenylephrine 1 mg/mL, 5 mL Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0021-05.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V299000·2022-05-04
Western Star 47X and 49X trucks recall for brake caliper safety
Brake caliper mounting bolts may loosen or detach on certain 2022-2023 Western Star 47X and 49X trucks, reducing brake performance. Dealers will inspect and tighten the bolts free of charge.
Product
WESTERN STAR — WESTERN STAR 49X, 47X
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0992-2022·2022-05-04
PrisMax System software causes unalerted treatment parameter reversion
The PrisMax System may revert custom treatment parameters to default values without notifying the operator when the Same Patient function is used. This could cause patients to receive unintended treatment settings.
Product
PrisMax System, Product Code 955724
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1012-2022·2022-05-04
Drager Infinity CentralStation Software Temporary Monitoring Functionality Loss
Drager is recalling Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12 due to a temporary loss of central monitoring functionality. The software is used for patient monitoring with wireless telemetry devices.
Product
Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12. For patient monitoring with Infinity M300 wireless telemetry devices.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0809-2022·2022-05-04
Prescription Injectable ST-1 Recalled for Manufacturing Process Control Failures
Olympia Compounding Pharmacy is recalling 525 vials of ST-1, a prescription injectable medication, due to manufacturing control failures.
Product
ST-1, Papaverine 30 mg/mL . Phentolamine 1.5 mg/mL . Alprostadil 50 mcg/ml, 10 mL Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0011-10.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0828-2022·2022-05-04
FDA recalls NAD+ powder due to failed reconstitution
Olympia Compounding Pharmacy is recalling NAD+ powder vials nationwide because they fail to reconstitute properly. Affected lot F41116 has a beyond-use date of 6/16/2022.
Product
NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder for reconstitution, Multi-Dose 500 mg Per Vial, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0083-00
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0798-2022·2022-05-04
Compounding Pharmacy Recalls Injectable Medication Vials for Manufacturing Quality Failures
Olympia Compounding Pharmacy recalls 1,871 multi-dose vials of QM-2 injectable medication due to failure to properly investigate manufacturing monitoring excursions prior to October 2021. No illnesses reported.
Product
QM-2 Papaverine 30 mg/mL. Phentolamine 3 mg/mL . Alprostadil 60 mcg/mL . Atropine 0.2 mg/mL, Multi-Dose 10 mL vial, Rx Only Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC: 73198-0018-10.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0800-2022·2022-05-04
FDA Recalls Compounded Injectable Drug Formula F9 Due to CGMP Violations
The FDA is recalling Formula F9, a compounded injectable medication, due to manufacturing control failures. Environmental and personnel monitoring protocols were not properly followed, which could allow contamination.
Product
Formula F9, Papaverine 0.9mg/ml . Phentolamine 0.1mg/ml . PGE 20mcg/mL Atropine 0.01mg/ml, Multi-Dose 10 ml vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC: 73198-0004-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0816-2022·2022-05-04
FDA Recalls Compounded Injectable Drug Due to Manufacturing Control Failure
Olympia Compounding Pharmacy is recalling a multi-drug injectable product nationwide due to manufacturing control deviations. The facility failed to properly investigate environmental and personnel monitoring excursions prior to October 2021.
Product
FA, Papaverine 20 mg/mL . Phentolamine 2 mg/mL . Alprostadil 20 mcg/mL . Atropine 0.2 mg/mL, 10 mL Multi-Dose vial, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0006-10.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1000-2022·2022-05-04
NeuMoDx COVID-19 test cartridges recalled for false positive risk
NeuMoDx Molecular is recalling diagnostic cartridges used in COVID-19 and flu/RSV tests because of potential for false positive SARS-CoV-2 results, which could lead to incorrect patient management.
Product
NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems with either of the following assays: NeuMoDx SARS CoV-2 Test Strip (REF 300800) NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip (REF 300900) NeuMoDx Laboratory Developed Tests (LDTs) for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1002-2022·2022-05-04
Boston Scientific SpaceOAR System Embolism Risk from Hydrogel Misplacement
FDA recalls Boston Scientific's SpaceOAR System due to risk of embolism from incorrect hydrogel placement during prostate cancer radiotherapy. Updated instructions provide verification steps for proper placement.
Product
SpaceOAR System, UPN SO-1010, SO-2101, SO-3101, and SO-4101. Used to temporarily position the anterior rectal wall away from the prostate during radiotherapy for prostate cancer to reduce the radiation dose delivered to the anterior rectum.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0824-2022·2022-05-04
Testosterone Cypionate Vials Recalled Due to Manufacturing Quality Control Deviation
Olympia Compounding Pharmacy recalls Testosterone Cypionate vials nationwide due to deviations in manufacturing quality monitoring procedures prior to October 2021.
Product
Testosterone Cypionate 200 mg/mL, (in Sesame Oil), Packaged in a) 10 mL Multi-Dose vial, NDC 73198-0055-10; b) 5 mL Multi-Dose vial, NDC 73198-0055-05, Rx Only, Olympia Pharmaceuticals 6700 Convoy Rd., Ste. 155, Orlando, FL 32835.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0997-2022·2022-05-04
CT Scanner Software Update May Display Incorrect Laser Positioning Coordinates
Siemens CT scanner imaging software upgraded to version VB60 may display incorrect laser offset coordinates during patient marking. Fourteen units are affected in the United States.
Product
syngo.via RT Image Suite upgraded to VB60 running on SOMATOM go.Open Pro Model Number 11061670. Running on servers with syngo.via VB60 software after upgrade and CT scanners with syngo.CT VA40A after upgrade.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0797-2022·2022-05-04
Sermorelin Acetate Vials Recalled for Manufacturing Quality Control Deviations
Olympia Pharmaceuticals is recalling approximately 18,060 vials of Sermorelin Acetate distributed nationwide due to manufacturing quality control deviations in which monitoring excursions were not properly investigated. Patients should contact their healthcare provider.
Product
Sermorelin Acetate, Lyophilized powder for reconstitution, Multi-Dose vials, Packaged as a) 3 mg per vial, NDC 73198-0060-00; b) 9 mg NDC 73198-0059-00, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0794-2022·2022-05-04
FDA Recalls Lidocaine-Prilocaine Topical Cream for Manufacturing Practice Violations
Teva Pharmaceuticals initiated a voluntary recall of Lidocaine-Prilocaine Cream due to manufacturing practice violations. The recall affects 353,964 units distributed nationwide.
Product
Lidocaine 2.5% and Prilocaine 2.5% Cream, USP, packaged in a) 5 g tubes (NDC 0591-2070-72), b) 30 g tubes (NDC 0591-2070-30), Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA
Category
Drug
Distribution
Distributed nationwide