State

US Virgin Islands product recalls

72,940 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: 2026-09-09

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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4726–4750 of 73117

HighFDA (Devices)·Z-0193-2026·2025-10-22
Retractable collar solution sets recalled across many lots because sets may leak
Baxter is recalling 958,351 CLEARLINK System Continu-Flo solution sets with three luer activated valves and a retractable collar because the IV sets may leak.
Product
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractable Collar, 10 drops/mL, 120-inch (3.0 meters), Product Code 2C8537
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0167-2026·2025-10-22
Six foot display cables recalled over inadequate shielding and interference
Spacelabs Healthcare is recalling 8,179 six-foot DVI display cables because inadequate shielding may allow electromagnetic interference with other electronically sensitive medical devices in use.
Product
Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-01 Software Version: N/A Product Description: 6 foot DVI-I to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0186-2026·2025-10-22
PICC and gastrostomy tube packs recalled after being sterilized more than once
American Contract Systems is recalling PICC G-Tube convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits UDPG88W PICC G-TUBE PACK-230209
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0194-2026·2025-10-22
Three valve retractable collar sets recalled across many lots for leak potential
Baxter is recalling 1,167,120 CLEARLINK System Continu-Flo solution sets with three luer activated valves and a retractable collar because the IV sets may leak.
Product
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractable Collar, 10 drops/mL, 120-inch (3.0 meters), Product Code 2C8541
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0198-2026·2025-10-22
Fourteen inch extension sets recalled from one lot because sets may leak
Baxter is recalling 2,304 CLEARLINK System straight-type extension sets with a retractable collar from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 14-inch (35 centimeters), Product Code 2C8632
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0174-2026·2025-10-22
Cystoscopy procedure packs recalled after being sterilized more than once
American Contract Systems is recalling cysto convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X CYSTO PACK - 205972 IHCY10Y CYSTO PACK MHCY35AE CYSTO PACK- 212487 PLBY52E CYSTO PACK UDCY31Z CYSTO PACK - 206047 UICY28L MOR CYSTO PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0108-2026·2025-10-22
Flow diverter devices recalled over tantalum defect affecting vessel wall apposition
MicroVention is recalling 467 FRED and FRED X flow diverters over a manufacturing issue with tantalum length or attachment that may leave the device incompletely open or poorly apposed.
Product
Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536, FRED3511, FRED5014, FRED3516, MV-F451827; FRED X 27, REF: XFRED4017-MVE, XFRED4528-MVE, MV-F501427X, XFRED4518-MVE, XFRED5526-MVE, XFRED4539-MVE,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0158-2026·2025-10-22
Humidifier devices recalled because power loss alert sounds under two minutes
Fisher & Paykel is recalling 51,144 Airvo 2 and myAirvo 2 humidifiers because an unintentional power disconnection may sound an audible alert for less than 120 seconds.
Product
Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0180-2026·2025-10-22
Angiography procedure packs recalled after being sterilized more than once
American Contract Systems is recalling angiography and coronary convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W ANGIOGRAPHY PACK MHCA98AK CORONARY ANGIO PACK- 205991 RCAN45C ANGIO CUSTOM RCH UDCO10F CVL CORONARY PACK 219224
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0181-2026·2025-10-22
Caesarean section packs recalled after being sterilized more than once
American Contract Systems is recalling C-section convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description FHCP08Y C SECTION PK HICS50I C-SECTION PACK HSCB90B C-SECTION BASIN PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0199-2026·2025-10-22
Extension IV sets recalled from one lot because the sets may leak
Baxter is recalling 16,416 CLEARLINK System straight-type extension sets from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 7.9-inch (20 centimeters), Product Code 2C8634
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0144-2026·2025-10-22
LGX preconnect pumps recalled over inflation and deflation performance issues
Boston Scientific is recalling 490 LGX Preconnect devices with TENACIO Pump and InhibiZone because of the potential for inflation or deflation performance issues or difficulties.
Product
LGX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404450 (12CM PS IZ), (2) 72404451 (15CM PS IZ), (3) 72404452 (18CM PS IZ), (4) 72404453 (21CM PS IZ), (5) 72404455 (12CM IP IZ), (6) 72404456 (15CM IP IZ), (7) 72404457 (18CM IP IZ), (8) 72404458 (21CM IP IZ);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0146-2026·2025-10-22
Electrosurgical units recalled over manufacturing defects that may cause adverse events
Lutronic is recalling 7,490 XERF EFFECTOR 60 electrosurgical units because manufacturing defects in devices made between April and August 2025 can on rare occasions result in adverse events.
Product
XERF EFFECTOR 60. Electrosurgical unit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0178-2026·2025-10-22
Head and neck procedure packs recalled after being sterilized more than once
American Contract Systems is recalling ENT and head and neck convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description RCEN25B ENT SDSC 0246972 RCHN27D HEAD AND NECK RCH 0246951
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0202-2026·2025-10-22
Three valve solution sets recalled from one lot because sets may leak
Baxter is recalling 12,720 CLEARLINK System Continu-Flo solution sets with three luer activated valves from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 120-inch (3.0 meters), Non-DEHP, Product Code 2R8537
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0203-2026·2025-10-22
Paclitaxel infusion sets recalled from one lot because IV sets may leak
Baxter is recalling 27,072 CLEARLINK System Paclitaxel Sets from one lot because the IV sets may leak.
Product
CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micron Filter, CLEARLINK Luer Activated Valve, 10 drops/mL, 107-inch (2.7 meters), Product Code 2R8858
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0134-2026·2025-10-22
Cyclodialysis surgical instruments recalled over compromised sterile packaging integrity
Iantrek is recalling 1,262 CycloPen Microinterventional Cyclodialysis Systems over the potential for compromised integrity of the sterile packaging.
Product
Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product Description: The CycloPen Microinterventional Cyclodialysis device is a manual surgical instrument used for the ab-interno construction or modification of a cyclodialysis, followed by delivery of
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0155-2026·2025-10-22
Ultrasound systems recalled over inaccurate liver steatosis measurement values
GE is recalling 65 LOGIQ P10 series systems running software R4.5.7 because the Ultrasound-Guided Attenuation Parameter measurement may display inaccurate liver steatosis values.
Product
LOGIQ P10 series with software version R4.5.7 Model Number 5877534
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0177-2026·2025-10-22
Central line insertion kits recalled after being sterilized more than once
American Contract Systems is recalling 32,433 adult central line insertion supply kits that were re-gassed after a nonconformance, without validation for multiple sterilization cycles.
Product
Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE INSERTION SUPPLY KIT UICL44R ADULT CENTRAL LINE INSERTION SUPPLY KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0132-2026·2025-10-22
Omnipod 5 app recalled because magnifying a field duplicates typed digits
Insulet is recalling 174,013 units of the Omnipod 5 iOS app because using the iPhone magnifier on a manual entry field while typing can duplicate a digit.
Product
The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature of the iPhone, while simultaneously selecting a single number on the keyboard.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0192-2026·2025-10-22
Continu-Flo solution sets recalled across six lots because sets may leak
Baxter is recalling 473,040 CLEARLINK System Continu-Flo solution sets across six lots because the IV sets may leak.
Product
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 112-inch (2.8 meters), Product Code 2C8519
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0172-2026·2025-10-22
General and laparotomy packs recalled after being sterilized more than once
American Contract Systems is recalling general, chest, laparotomy and interventional radiology convenience packs that were re-gassed after a sterilization nonconformance.
Product
Medical convenience kits Item number/ Product description AKGN82E GENERAL AMCB08Y CHEST BREAST PACK ANBP10AC BASIC PACK - 205939 ANIR77AM INTERVENTIONAL RADIOLOGY PACK - 205953 CFLA39G LAPAROTOMY PACK CIBL33I BASIC LAP PACK EVMN24E MINOR ESC EVST48E STARTER FDTA11AA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0182-2026·2025-10-22
Radiology procedure packs recalled after being sterilized more than once
American Contract Systems is recalling radiology convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0142-2026·2025-10-22
CX preconnect pumps recalled over inflation and deflation performance issues
Boston Scientific is recalling 2,288 CX Preconnect devices with TENACIO Pump and InhibiZone because of the potential for inflation or deflation performance issues or difficulties.
Product
CX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404430 (12CM PS IZ), (2) 72404431 (15CM PS IZ), (3) 72404432 (18CM PS IZ), (4) 72404433 (21CM PS IZ), (5) 72404434 (24CM PS IZ), (6) 72404435 (12CM IP IZ), (7) 72404436 (15CM IP IZ), (8) 72404437 (18CM IP IZ), (9)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0191-2026·2025-10-22
Non-vented IV solution sets recalled from one lot because sets may leak
Baxter is recalling 1,440 CLEARLINK System non-vented solution sets from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, 10 drops/mL, 100-inch (2.5 meters), Product Code 2C8425
Category
Medical Device
Distribution
Distributed nationwide