State

US Virgin Islands product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27276–27300 of 73754

HighFDA (Devices)·Z-0244-2021·2020-10-28
ICU Medical Recalls 128-inch Primary Sets Due to Seal Defect
ICU Medical is recalling specific lots of 128-inch primary sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
Product
128" (325 cm) Appx 16.6 ml, 15 Drop Primary Set w/2 MicroClave, Remv 2 Gang 4-Way Clave Stopcock, Rotating Luer, 2 Ext. 1 unit per pouch, 50 multivac pouches per case.UDI:(01)10887709011691(17)250201(30)50(10)4711125;(01)10887709011691(17)250201(30)50(10)4718711. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0233-2021·2020-10-28
ICU Medical Recalls 139-inch Admin Sets Due to Potential Seal Defect
ICU Medical is recalling specific lots of 139-inch intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
Product
139" (353 cm) 15 Drop Admin Set w/3 MicroClave Clear, 4-Way Stopcock, 3-Port NanoClave Manifold w/Check Valve, Spin Luer, 2 Ext. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709121147(17)250101(30)25(10)4556713; (01)10887709121147(17)250101(30)25(10)4603383…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0149-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Suture Anchors Due to Seal Defects
Smith & Nephew is recalling OSTEORAPTOR 2.3 suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.3 W/ 1 UB COBRAID BLACK-Absorbable Suture anchor Product Number: 72201992
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0168-2021·2020-10-28
Smith & Nephew Recalls Absorbable Suture Anchors Due to Seal Defects
Smith & Nephew is recalling HEALICOIL RSB SA absorbable suture anchors because improper packaging seals may breach the sterile barrier.
Product
HEALICOIL RSB SA 4.75MM W/1 UT & 1 UB BL-- Absorbable Suture anchor Product Number: 72203704
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0225-2021·2020-10-28
ICU Medical Recalls Intravascular Administration Sets Due to Manufacturing Defect
ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent a proper seal.
Product
112 IN (284cm) APPX 14.7ml 15 DROP SET 2 MicroClave, Remv 3-Port NanoClave Manifold, BCV.1 unit per pouch, 25 pouches per case. UDI:(01)10887709088501(17)250201(30)25(10)4733705. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0163-2021·2020-10-28
Smith & Nephew Recalls TWINFIX ULTRA HA Absorbable Suture Anchors
Smith & Nephew is recalling TWINFIX ULTRA HA absorbable suture anchors due to improper or incomplete packaging seals that may breach the sterile barrier.
Product
TWINFIX ULTRA HA 5.5 W/2 UB BLUE & BLK- Absorbable Suture anchor Product Number: 72202626
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0039-2021·2020-10-28
Genesis Hand Sanitizer Gel Recalled for CGMP Deviations
Genesis Partnership Company SA is recalling 5,040 bottles of hand sanitizer gel due to manufacturing deviations in a facility that produced sub-potent products.
Product
Genesis Hand Sanitizer Gel, Topical Solution, Non Sterile Solution, 1 gallon (3785 mL) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, NDC 74484-002-04, UPC 7401037203427.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0038-2021·2020-10-28
Genesis Hand Sanitizer Gel Recalled for CGMP Deviations
Genesis Partnership Company SA is recalling 15,000 bottles of Genesis Hand Sanitizer Gel due to manufacturing deviations in a facility that produced sub-potent products.
Product
Genesis Hand Sanitizer Gel, Topical Solution, Non Sterile Solution, 240 mL (8 FL OZ.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, NDC 74484-002-02, UPC 7401037205773.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0124-2021·2020-10-28
Quidel Recalls Sofia SARS Antigen FIA Package Inserts for Labeling Errors
Quidel Corporation is recalling package inserts for the Sofia SARS Antigen FIA test because instructions referencing specific viral transport media may lead to false-positive results.
Product
Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay that is used with the Sofia and Sofia 2 instrument intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0159-2021·2020-10-28
Smith & Nephew Recalls TWINFIX ULTRA Absorbable Suture Anchors Due to Seal Defects
Smith & Nephew is recalling TWINFIX ULTRA absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
TWINFIX ULTRA PLLA HA 4.5MM W/ NEEDLES- Absorbable Suture anchor Product Number: 72202612
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0281-2021·2020-10-28
Sobel Westex Disposable Isolation Gowns Recalled for Performance Failures
Sobel Westex is recalling 3,380,850 disposable isolation gowns because they did not meet all performance test requirements. The gowns were distributed nationwide in the U.S.
Product
SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP non woven laminate with PE Film - Product Usage: use in patient/healthcare personnel interactions. AAMI Level II isolation gowns are intended for relatively low risk procedures, including blood draws, lab work…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0173-2021·2020-10-28
Smith & Nephew Recalls Healicoil Absorbable Suture Anchors for Seal Defects
Smith & Nephew is recalling Healicoil absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BL- Absorbable Suture anchor Product Number: 72203801
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0141-2021·2020-10-28
Smith & Nephew Recalls TWINFIX AB 5.0 Suture Anchors Due to Seal Defects
Smith & Nephew is recalling TWINFIX AB 5.0 Suture Anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
TWINFIX AB 5.0 SUTR ANCHR W/2 38 ULTRA-Absorbable Suture anchors Product Number:72200777
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0037-2021·2020-10-28
Panagel Hand Sanitizer Recalled for CGMP Deviations and Sub-Potent Ethanol Risk
Genesis Partnership Company SA is recalling 33,480 bottles of Panagel Hand Sanitizer due to CGMP deviations and potential sub-potent ethanol levels.
Product
Panagel Hand Sanitizer, 70% Alcohol,16 Fl. Oz. (472 mL) bottle, Made in Guatemala, Distributed by Central Med Distribution, 6100 Hollywood Blvd, Hollywood FL 33024, NDC 78384-001-04, UPC 378384000016.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0155-2021·2020-10-28
Smith & Nephew Recalls TWINFIX ULTRA Absorbable Suture Anchors Due to Seal Defects
Smith & Nephew is recalling TWINFIX ULTRA absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
TWINFIX ULTRA 5.5MM PLLA/HA 2 UBWHT/BL--Absorbable Suture anchor Product Number: 72202602
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0117-2021·2020-10-28
Encore Medical Recalls Mislabeled AltiVate Shoulder Socket Inserts
Encore Medical is recalling 15 AltiVate Reverse Small Socket Inserts due to mislabeling. The error may cause surgery delays or the need for revision surgery.
Product
AltiVate Reverse Small Socket Insert, 44mm Semi Constrained - E-Plus, Part Number: 509-03-044 - Product Usage: Per IFU, DJO Surgical shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0202-2021·2020-10-28
ICU Medical Recalls Smallbore Intravascular Administration Sets Due to Seal Defect
ICU Medical is recalling specific lots of smallbore intravascular administration sets because a manufacturing defect may prevent a proper seal.
Product
8" (20 cm) Appx 0.53 ml, Smallbore Ext Set w/MicroClave Clear, 0.2 Micron Filter, NanoClave T-Connector, Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709075334(17)250101(30)50(10)4572784. The Intravascular Administration Set is a single…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0282-2021·2020-10-28
Fujifilm Synapse PACS Software Version 5.6.1 Recalled for CT Measurement Error
Fujifilm is recalling Synapse PACS Software Version 5.6.1 because certain CT studies may report inaccurate 3D Sphere MAX values.
Product
Synapse PACS Software Version 5.6.1 - Product Usage: intended for use as a web based application on an off-the shelf PC which meets or exceeds minimum specifications and is networked with a FUJIFILM Synapse PACS server.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0041-2021·2020-10-28
Killz Germz Hand Sanitizer Recalled for Sub-Potent Ethanol Levels
Genesis Partnership Company SA is recalling Killz Germz Hand Sanitizer because testing showed ethanol levels as low as 62%, below the labeled 70% claim.
Product
Killz Germz Hand Sanitizer, Alcohol Gel, 1 Gallon (128 fl. oz.) bottle, Manufactured by Genesis Partnership Company S.A., Guatemala, For: Killz Germz, LLC., 1912 R street NW, Washington DC 20009, NDC 74625-003-05, UPC 7401037203427.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0166-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR CRVD 2.3 SA UB COBRD BLACK- Absorbable Suture anchor Product Number: 72203291
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0165-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- Absorbable Suture anchor Product Number: 72203290
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0152-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE -Absorbable Suture anchor Product Number: 72201995
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0160-2021·2020-10-28
Smith & Nephew Recalls TWINFIX ULTRA Absorbable Suture Anchors
Smith & Nephew is recalling TWINFIX ULTRA absorbable suture anchors due to improper or incomplete packaging seals that may breach the sterile barrier.
Product
TWINFIX ULTRA PLLA HA 5.5MM W/ NEEDLES- Absorbable Suture anchor Product Number: 72202616
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0151-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Issues
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.9 W/ 1 UB COBRAID BLUE -Absorbable Suture anchor Product Number: 72201994
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0150-2021·2020-10-28
Smith & Nephew Recalls OSTEORAPTOR Absorbable Suture Anchors Due to Seal Defects
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
Product
OSTEORAPTOR 2.3 W. UB COBRAID BLUE-Absorbable Suture anchor Product Number: 72201993
Category
Medical Device
Distribution
Distributed nationwide