State

US Virgin Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33576–33600 of 73900

HighFDA (Food)·F-1432-2019·2019-06-05
Suja Organic Kombucha Recalled Due to Glass Fragments
Suja Life LLC is recalling 31,079 cases of Organic Kombucha Variety Packs because consumers reported finding pieces of glass in the bottles.
Product
Suja Organic Kombucha - Variety Pack: 6 x 15.2 oz. glass bottle; 2 each of Ginger Lemon, Mixes Berries and Peach Ginger UPC 818617020737; DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE, CA 92056 CERTIFIED ORGANIC BY CCOF SUJAJUICE.COM
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1674-2019·2019-06-05
Maquet Getinge Custom Neonatal ECC Tubing Sets Recalled for Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific neonatal extracorporeal circulation tubing sets because a design feature may prevent proper sterilization gas flow, potentially compromising sterility.
Product
Maquet Getinge-BEQ-TOP 50900 Custom ECC Pack-Neonatal ¿ Material: 709000069R02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1589-2019·2019-06-05
Maquet Getinge Custom Tubing Sets Recalled for Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design flaw may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-TOP 50100 CHOSA 1/4" ECC PACK Material: 701067837
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1611-2019·2019-06-05
Maquet Getinge-T 8030 High Flow Pigtail Tubing Recalled for Sterility Assurance Issues
Maquet Cardiovascular is recalling specific Custom Tubing Sets for Extracorporeal Circulation because a design configuration may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-T 8030 4 in High Flow Pigtail Material: 709000366
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1675-2019·2019-06-05
Maquet Custom Tubing Sets Recalled Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling Custom Tubing Sets for Extracorporeal Circulation because a design flaw may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-TOP 50903 Custom ECC Pk-Pdtrc 3/8 - Material: 709000078R01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1661-2019·2019-06-05
Maquet Getinge Custom Tubing Sets Recalled Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge- BEQ-TOP 41201 ECC 3/8 Pump Pack Wake For Material: 701064867R01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1564-2019·2019-06-05
Maquet Getinge-BEQ-TOP 41201 ECC 3/8 PUMP PAC Recall for Sterility Assurance
Maquet Cardiovascular is recalling specific ECC pump packs because a design flaw may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-TOP 41201 ECC 3/8 PUMP PAC Material: 701064867
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1489-2019·2019-06-05
Change Healthcare Recalls Horizon Cardiology Hemo Software Due to Medication Discrepancies
Change Healthcare Israel Ltd. is recalling 125 units of Horizon Cardiology Hemo software because it fails to notify users of medication discrepancies, potentially affecting patient data and reports.
Product
Horizon Cardiology Hemo
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V417000·2019-06-05
Thor Motor Coach Recalls 2019-2020 Magnitude and Omni Motorhomes for Fire Risk
Thor Motor Coach is recalling 2019-2020 Magnitude and Omni motorhomes because wires in the electrical junction box may contact an extra screw, increasing the risk of an electrical short circuit and fire.
Product
THOR MOTOR COACH — THOR MOTOR COACH MAGNITUDE, OMNI
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1572-2019·2019-06-05
Maquet Getinge Neonate Tubing Sets Recalled for Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific neonate tubing sets because a design feature may prevent sterilization gas from reaching all parts of the device.
Product
Maquet Getinge-BO-T 46200 3/16" x 1/4" Neonate Pack Material: 701065620
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1560-2019·2019-06-05
Maquet Cardiovascular Recalls Custom Tubing Sets for Extracorporeal Circulation
Maquet Cardiovascular is recalling custom tubing sets for extracorporeal circulation because a design flaw may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-T 27904 3/8 TRANSPORT PACK Material:701064804
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1682-2019·2019-06-05
Teleflex Medical Recalls RUSCH LASERTUBE Due to Laser Guard Foil Separation
Teleflex Medical is recalling 1,787 units of RUSCH LASERTUBE (Rubber) because the laser guard foil partially separated or detached at the edges.
Product
RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1655-2019·2019-06-05
Maquet Getinge Custom Tubing Sets Recalled for Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization gas flow, compromising sterility.
Product
Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1663-2019·2019-06-05
Maquet Getinge Custom Tubing Sets Recalled for Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific Custom Tubing Sets for Extracorporeal Circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge- (1)Material: 701065765R01 BO-TOP 36504 Adult ECC Pack (2)Material: 701065765R02 BO-TOP 36504 Adult ECC Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1597-2019·2019-06-05
Maquet Getinge ECC Pump Pack Recall Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific ECC Pump Packs because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-T 30914 ECC Pump Pack 1/4" Material: 709000011
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1518-2019·2019-06-05
Maquet Getinge Tubing Sets Recalled Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-TOP 1601#QUADROX iD - Pack Material:701052285
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1610-2019·2019-06-05
Maquet Getinge Tubing Sets Recalled Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-T 5914 TCH ¿ Inch Change Kit Material: 709000334
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1582-2019·2019-06-05
Maquet Getinge Custom Tubing Sets Recalled Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-T 8068 1/4" WITH BRIDGE Material: 701066883
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1632-2019·2019-06-05
Maquet Getinge Custom Tubing Sets Recalled Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling custom tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-TOP 22600 ECC QUADROX ID 3 Material:701049440R01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1607-2019·2019-06-05
Maquet Getinge-BEQ-T 53400 Adaption Pack Recall for Sterility Assurance Issues
Maquet Cardiovascular is recalling specific batches of Custom Tubing Sets for Extracorporeal Circulation because the stopcock design may prevent proper sterilization.
Product
Maquet Getinge-BEQ-T 53400 Adaption Pack Material: 709000213
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1620-2019·2019-06-05
Maquet Getinge Custom Tubing Sets Recalled Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-T 9410 Lurie Chldns Small 1/4 Material: 709000430
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1628-2019·2019-06-05
Maquet Pediatric Extracorporeal Circulation Tubing Sets Recalled for Sterility Concerns
Maquet Cardiovascular is recalling specific pediatric tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-T 4932 Mercy Adaptation Pk Pediatric Material:709000520
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2019·2019-06-05
Maquet Getinge-BEQ-TOP 35503 SGD Pack Recall Due to Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific Custom Tubing Sets for Extracorporeal Circulation because a design feature may prevent proper sterilization, potentially compromising sterility.
Product
Maquet Getinge-BEQ-TOP 35503 SGD Pack Material: 701068797
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1676-2019·2019-06-05
Maquet Getinge Adult ECC Tubing Sets Recalled for Sterility Assurance Concerns
Maquet Cardiovascular is recalling specific Adult ECC Packs because a design feature may prevent sterilization gas from reaching all fluid paths, potentially compromising sterility.
Product
Maquet Getinge BO-TOP 28903 Adult ECC Pack Material: -709000093R01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1495-2019·2019-06-05
ThermaCare HeatWraps Recalled for Potential Skin Burn Risk
PF Consumer Healthcare is recalling ThermaCare HeatWraps because some units may produce higher-than-specified temperatures, posing a risk of skin burns or blisters.
Product
ThermaCare HEATWRAPS, ADVANCED BACK PAIN THERAPY, UPC 305733010037 - Product Usage: ThermaCare(R) HeatWraps are indicated in adults to provide heat therapy for the temporary relief of minor muscular and joint pains associated with overexertion, strains, sprains, and arthritis…
Category
Medical Device
Distribution
Distributed nationwide