State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

61001–61025 of 74011

HighFDA (Devices)·Z-0269-2014·2013-11-20
Philips IntelliSpace PACS 4.4 Software Recall for Image Storage Defect
Philips is recalling IntelliSpace PACS 4.4 software due to a timing issue that may prevent the system from storing additional images, potentially affecting clinical diagnoses.
Product
Philips brand IntelliSpace PACS 4.4, Image Management System; The system is a software package used with general purpose computing hardware to acquire, store, distribute, process and display images and associated data throughout a clinical environment. Product is manufactured…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0191-2014·2013-11-20
DePuy Mitek FMS Intermediary Tubing Recalled Due to Valve Malfunction
DePuy Mitek is recalling FMS Intermediary Tubing with One-Way Valve because the pillow valve may not perform as intended, potentially leading to patient cross-contamination.
Product
DePuy Mitek FMS Intermediary Tubing with One-Way valve Product Code: 281142 Product Usage: The Intermediary Tubing for FMS¿ Fluid Management Systems connects the Inflow Tubing to the arthroscopic sheath during arthroscopic procedures. The Polyvinyl Chloride (PVC) tubing…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0283-2014·2013-11-20
Hospira Recalls Plum A+ Infusers Due to Broken Pressure Sensor Pin
Hospira Inc. is recalling 179 Plum A+ Hyperbaric Infusion Systems because the distal pressure sensor pin may break, potentially preventing the detection of line occlusions.
Product
The Plum A+ Hyperbaric Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Hyperbaric Infusion System is designed to deliver parenteral, enteral…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0287-2014·2013-11-20
Hospira Recalls Plum A+ Infusion Systems Due to Broken Sensor Pin Risk
Hospira Inc. is recalling 182,971 Plum A+ Infusion Systems because a distal pressure sensor pin may break, potentially preventing the detection of line occlusions.
Product
The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Infusion System is designed to deliver parenteral, enteral, or epidural infusions…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0288-2014·2013-11-20
Hospira Recalls Plum A+3 Infusion Systems Due to Broken Sensor Pin Risk
Hospira is recalling 7,692 Plum A+3 Infusion Systems because a pressure sensor pin may break, potentially preventing the detection of line occlusions.
Product
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+3 Infusion System is designed to deliver parenteral, enteral, or epidural…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0135-2014·2013-11-20
Specialty Enzymes Recalls Cellulase and Protease Products for Chloramphenicol
Specialty Enzymes & Biotechnologies is recalling cellulase and protease products because they may contain low levels of chloramphenicol.
Product
Cellulase & Protease: APEX 10-639 A DIGESEB DIGESEB PLUS DIGESEB SUPER EB 10-14171 EB 10-16192 EB 12-11331 EB 12-9205 EB 14-14201 EB 15-13662 EB 18-13081 EB 7-12831 EB 7-12901 EB 7-14211 EB 8-15731 EL 5-7212 ENZIGEST N FIZYME # 1209 N GLOBAL 8-658 HERB…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0189-2014·2013-11-20
Baxter Recalls SIGMA SPECTRUM Infusion Pump LCD Screens for Discharge Failure
Baxter Healthcare is recalling 346 SIGMA SPECTRUM Infusion Pump LCD screens that failed to withstand electrostatic discharge.
Product
SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B) Product Usage: Intended to be used as a visual aid during the controlled administration of intravenous fluids. These fluids may include pharmaceutical drugs, blood, blood…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0272-2014·2013-11-20
Biotene Moisturizing Mouth Spray Recalled for Incorrect Ingredient Labeling
GlaxoSmithKline is recalling Biotene Moisturizing Mouth Spray because the label lists sorbitol, but the product does not contain it.
Product
Biotene Moisturizing Mouth Spray, with xylitol, For dry mouth symptom relief, 44.3ml/1.5 FL. OZ., Sugar Free Sweetened with xylitol and sorbitol, GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108. Biotene Mouth Spray is used for the treatment of dry mouth
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0273-2014·2013-11-20
Nobel Biocare Recalls Osseocare Pro Dental Devices Due to Malfunction Risk
Nobel Biocare is recalling Osseocare Pro dental consoles because they may malfunction when used with a specific iPad software version.
Product
Osseocare Pro Console & Set Osseocare Pro, Model 1600870-001, 1700470-001, and 1700471-001. Device Name: Osseocare Pro console & Set Osseocare Pro. Model: 1600870-001, 1700470-001, 1700471-001. Marketing status: Class I, under K092214. Device description: Software-based…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0142-2014·2013-11-20
Apex Energetics Recalls Four Supplements Due to Chloramphenicol Contamination
Apex Energetics is recalling four dietary supplements because they may contain trace amounts of the antibiotic chloramphenicol from a raw material supplier.
Product
SuperDigestZyme (Z22), Plant Enzyme and Cofactor Dietary Supplement, 100 tablets
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0199-2014·2013-11-20
Anspach Effort Recalls Cutting Bur Chart Due to Labeling Error
Anspach Effort, Inc. is correcting labeling on its Cutting Bur Chart and related manuals because a claim about cutting biometals was not part of the device's intended use.
Product
Cutting Bur Chart (part number 20-0019) utilized with the Electric and Pneumatic Motor Systems including: MicroMax Motor Systems, XMax Motor Systems, EMax2 Motor Systems, and Emax2Plus Motor Systems, all models and serial numbers. Product Usage: Indication for use is…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0137-2014·2013-11-20
Specialty Enzymes Recalls Xylanase 150,000 Due to Chloramphenicol Contamination
Specialty Enzymes and Biotechnologies is recalling Xylanase 150,000 because it may contain low levels of chloramphenicol.
Product
XYLANASE 150,000
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0190-2014·2013-11-20
Advanced Sterilization Products Recalls Sterrad 100NX Sterilizers Due to Odor Reports
Advanced Sterilization Products is recalling Sterrad 100NX sterilizers because healthcare workers detected odors, potentially linked to vacuum pump oil breakdown.
Product
Sterrad 100NX, Product Code: 10104. Used to sterilize heat and moisture sensitive reusable medical devices.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0133-2014·2013-11-20
Specialty Enzymes Recalls Cellulase Products Due to Chloramphenicol Contamination
Specialty Enzymes and Biotechnologies is recalling cellulase and protease products because they may contain low levels of chloramphenicol.
Product
Cellulase: ACTA 4-702 APEX 17-6262 APEX 6-9762 ARTH EB 10831 BETA GLUCANASE 1000 BROOK 8-352 CELLULASE 1000 CELLULASE 4000 CELLULASE CONC. CENTURY 7-152 CLENZSEB DIGESEB DIGESEB PB DIGESEB PLUS DIGESEB PLUS 401 DIGESEB SUPER DIGESEB SUPER 118 EB 10-14081 EB…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0200-2014·2013-11-20
Anspach Effort Recalls Pneumatic Systems Operating Manual and Product Catalog
Anspach Effort, Inc. is correcting labeling on its Pneumatic Systems Operating Manual and Product Catalog because a claim regarding the device's capability to dissect biometals, bioplastics, and cement was found to be inaccurate.
Product
Product Catalog (part number 20-0020) utilized with the Electric and Pneumatic Motor Systems including: MicroMax Motor Systems, XMax Motor Systems, EMax2 Motor Systems, and Emax2Plus Motor Systems, all models and serial numbers. Product Usage: Indication for use is cutting…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0274-2014·2013-11-20
SpineFrontier Recalls S-LIFT Extension Shims Due to Fit Variation
SpineFrontier, Inc. is recalling 67 S-LIFT Extension Shims because they may not fit down all retractor blades, potentially interfering with surgical procedures.
Product
S-LIFT Extension Shims Extension shims are manufactured from grade 5 titanium and are curved, rectangular slabs which have four protrusions used for ratcheting. They come in straight and pointed varieties, either with or without a tab containing an additional bend. Extension…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0277-2014·2013-11-20
Zimmer Recalls Hip Stems Due to Sterile Barrier Integrity Testing
Zimmer, Inc. is recalling VerSys Hip System femoral stems because historic packaging validations indicated a need for additional testing to ensure sterile barrier integrity.
Product
VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys Heritage Hip System Revision Femoral Stems. Indicated for total hip arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0187-2014·2013-11-20
St. Jude Medical Recalls Safire Duo Ablation Catheters Due to Connector Error
St. Jude Medical is voluntarily recalling 46 Safire Duo Ablation Catheters because they have a cable connector configuration that differs from the intended design.
Product
Safire Duo Ablation Catheter MediGuide Enabled, REF A700240 and A700238, Rx only, Sterile EO. Intended for creating endocardial lesions during cardiac ablation procedures (mapping, stimulation and ablation) for the treatment of typical atrial flutter.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0141-2014·2013-11-20
Apex Energetics Recalls Four Supplements Due to Chloramphenicol Contamination
Apex Energetics is recalling four dietary supplements because they may contain trace amounts of the antibiotic chloramphenicol.
Product
GlutenFlam (K-52) Enzyme & Bioflavonoid Dietary Supplement, 60 vegetarian capsules
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0271-2014·2013-11-20
Siemens syngo.plaza Image Processing System Recalled for Patient Data Merge Error
Siemens is recalling 19 syngo.plaza image processing systems because a software function can cause unintended patient data merges when transferring data between systems.
Product
Siemens syngo.plaza image processing system image processing radiological system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0138-2014·2013-11-20
Metagenics Recalls Spectrazyme Due to Potential Chloramphenicol Contamination
Metagenics is recalling Spectrazyme supplements because raw materials may contain the antibiotic chloramphenicol. The recall covers products distributed in the US and several international markets.
Product
Spectrazyme, 180 count, 60 count, 12 bottles/case, 20000 tablets/box, 14000 capsules/pail.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0183-2014·2013-11-20
Applied Medical Recalls Inzii Tissue Retrieval Bags Due to Packaging Punctures
Applied Medical is voluntarily recalling Inzii Tissue Retrieval Bags because packaging punctures could compromise the sterile barrier, posing a theoretical risk to patients.
Product
Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue Retrieval Bag, Model Number CD004, is classified as a Class II device. It was cleared to market via 510(k) filing K060051. The retrieval bag is a disposable specimen retrieval bag intended for use as…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0140-2014·2013-11-20
Ultra Laboratories Recalls Digestive Health Capsules Due to Chloramphenicol Contamination
Ultra Laboratories is recalling Digestive Health capsules because a raw material may have been contaminated with chloramphenicol.
Product
Digestive Health, 90 vegetable capsules
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0134-2014·2013-11-20
Specialty Enzymes Recalls Protease Products Due to Chloramphenicol Contamination
Specialty Enzymes & Biotechnologies is recalling specific protease products because they may contain low levels of chloramphenicol.
Product
Protease: APEX 10-7082 CENTURY 7-152 EB 2-14511 EB 5-16901 EB 8-14861 EB 9-14191 EXCLZYME EXCLZYME EN GLOBAL 8-658 HFN 7-7113 META 10-185 MHNHEM 2-158 PEPZYME AG PROTEASE - 1000 PROTEASE 250,000 SEB PRO FP 500 SEB PRO FP 600 SYS 7-7742 UT 11-216 N…
Category
Food
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0198-2014·2013-11-20
Anspach Effort Pneumatic Systems Operating Manual Labeling Correction
Anspach Effort is correcting labeling on Pneumatic Systems Operating Manuals to remove unverified claims about cutting biometals, bioplastics, and cement.
Product
Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the Pneumatic Motor Systems including: BlackMax Motor Systems, MicroMax Systems and XMax Motor Systems all models and serial numbers. Product Usage: Indication for use is cutting and shaping bone.
Category
Medical Device
Distribution
Distributed nationwide