State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54576–54600 of 74002

HighFDA (Drugs)·D-693-2015·2015-04-29
Attix Pharmaceuticals Recalls Fulvestrant API Due to Penicillin Cross-Contamination Risk
Attix Pharmaceuticals is recalling Fulvestrant active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.
Product
Fulvestrant active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-846-2015·2015-04-29
Attix Pharmaceuticals Recalls Podophyllum Resin Due to Penicillin Cross-Contamination Risk
Attix Pharmaceuticals is recalling Podophyllum Resin active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.
Product
Podophyllum Resin active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-669-2015·2015-04-29
Attix Pharmaceuticals Recalls Exemestane API Due to Penicillin Cross-Contamination Risk
Attix Pharmaceuticals is recalling Exemestane active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging. The product was distributed nationwide to compounding pharmacies and research organizations.
Product
Exemestane active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1499-2015·2015-04-29
Wright Medical Recalls Crosscheck Plating System Due to Specification Defects
Wright Medical Technology is recalling 151 units of the Crosscheck Plating System because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.
Product
CROSSCHECK(R) Plating system, Utility Plate, 7-Hole, REF CCP-UTN7. Orthopedic use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-664-2015·2015-04-29
Attix Pharmaceuticals Recalls Etodolac Due to Penicillin Cross-Contamination Risk
Attix Pharmaceuticals is recalling Etodolac active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.
Product
Etodolac active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1455-2015·2015-04-29
DBX Mix Bone Void Filler Recalled for Potential Packaging Seal Defect
Musculoskeletal Transplant Foundation is recalling 25 units of DBX Mix bone void filler because the outer packaging seal may not be fully intact.
Product
DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1510-2015·2015-04-29
Specialty Appliance Works Recalls Universal Nuts for Incorrect Stainless Steel Material
Specialty Appliance Works is recalling Universal Nuts used in Herbst Appliances because they were made with 416 SS instead of the specified 303 SS.
Product
Upper Right Telescope Unibodies (5/pk) and Upper Left Telescope Unibodies (54/pk) A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1459-2015·2015-04-29
Exactech Recalls Equinoxe 44mm Short Humeral Head Shoulder Implants
Exactech, Inc. is recalling 112 Equinoxe 44mm Short Humeral Head shoulder implant components because incorrect outer and inner labeling may misidentify the device size.
Product
Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic shoulder implant component.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1516-2015·2015-04-29
PhotoMedex Recalls Iamin Medical Devices Due to Inconsistent Labeling
PhotoMedex, Inc. is recalling Iamin Moist Dressings and Hydrating Gel because their labeling does not match the intended uses approved by the FDA.
Product
Iamin Moist Dressing and the Iamin Hydrating Gel: intended to cover a wound or burn on the skin, provide a moist wound environment and protect against abrasion, friction, desiccation and contamination.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1503-2015·2015-04-29
Specialty Appliance Works Recalls Orthodontic Universal Nuts Due to Material Error
Specialty Appliance Works is recalling 14,428 Universal Nuts used in orthodontic Herbst Appliances because they were manufactured with 416 SS instead of the specified 303 SS.
Product
MiniScope Hst ROC Crown 15 Patient Kit, and MiniScope Herbst Crown 15 Patient Kit A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1509-2015·2015-04-29
Specialty Appliance Works Recalls Orthodontic Universal Nut Components
Specialty Appliance Works is recalling Universal Nut components for Herbst Appliances because they were made with 416 SS instead of the specified 303 SS.
Product
TS Crown Component 4UR (5/pk), TS Crown Component 5UR (5/pk), TS Crown Component 6UR (5/pk), TS Crown Component 4LR (5/pk), TS Crown Component 5LR (5/pk), TS Crown Component 6LR (5/pk), TS Crown Component 4UL (5/pk), TS Crown Component 5UL (5/pk), TS Crown Component 4LL (5/pk)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-967-2015·2015-04-29
Tarmac Recalls Well at Walgreens Comfort Gel for Antimicrobial Failure
Tarmac Products, Inc. is recalling Well at Walgreens Regular Strength Comfort Gel Cherry Flavor because the product failed the Antimicrobial Effectiveness Test.
Product
Well at Walgreens Regular Strength Comfort Gel Cherry Flavor, 12 fl oz (355 mL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-707-2015·2015-04-29
Attix Pharmaceuticals Recalls Homatropine Methylbromide Due to Penicillin Cross-Contamination Risk
Attix Pharmaceuticals is recalling Homatropine Methylbromide active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.
Product
Homatropine Methylbromide active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1466-2015·2015-04-29
Biomet Recalls Torque Limiting Handles for Spinal Fixation Devices
Biomet Spine is recalling 874 Torque Limiting Handles used in spinal fixation due to supplier component updates.
Product
Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage: Provides posterior fixation in the non-cervical spine with an interspinous fixation device.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1505-2015·2015-04-29
Specialty Appliance Works Recalls MiniScope Mechanical Set Universal Nuts
Specialty Appliance Works is recalling Universal Nuts for MiniScope Mechanical Sets because they were made with 416 stainless steel instead of the specified 303 stainless steel.
Product
Specialty MiniScope Mech. Set Size 18, Specialty MiniScope Mech. Set Size 21, and Specialty MiniScope Mech. Set Size 24 A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1502-2015·2015-04-29
Herbst Universal Nut Recalled for Incorrect Stainless Steel Material
Specialty Appliance Works is recalling Herbst Universal Nuts because they were manufactured with 416 SS instead of the specified 303 SS.
Product
Herbst Universal Nut which is used in a Herbst Appliance A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1504-2015·2015-04-29
Specialty Appliance Works Recalls Orthodontic Herbst Appliance Nuts
Specialty Appliance Works is recalling TS Herbst Nuts because they were manufactured with 416 stainless steel instead of the specified 303 stainless steel.
Product
TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts Universal (10/pk) A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1511-2015·2015-04-29
Specialty Appliance Works Recalls Orthodontic Universal Nut Components
Specialty Appliance Works is recalling TS ROC Crown Components because the Universal Nut was made with 416 SS instead of the specified 303 SS.
Product
TS ROC Crown Component 4UR (5/pk), TS ROC Crown Component 5UR (5/pk), TS ROC Crown Component 6UR (5/pk), TS ROC Crown Component 7UR (5/pk), TS ROC Crown Component 8UR (5/pk), TS ROC Crown Component 4LR (5/pk), TS ROC Crown Component 5LR (5/pk), TS ROC Crown Component 6LR (5/pk)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1508-2015·2015-04-29
Specialty Appliance Works Recalls Universal Nuts for Herbst Appliances
Specialty Appliance Works is recalling Universal Nuts used in Herbst orthodontic appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.
Product
LR Telescoping Cantilever Arms (5/pk) and LL Telescoping Cantilever Arms (5/pk) A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-844-2015·2015-04-29
Attix Pharmaceuticals Recalls Piperacillin Sodium Due to Missing Stability Data
Attix Pharmaceuticals is recalling Piperacillin Sodium active pharmaceutical ingredient because it was repackaged without data supporting the printed expiry date.
Product
Piperacillin Sodium active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-520-2015·2015-04-29
Attix Pharmaceuticals Recalls Amoxicillin Trihydrate Due to Missing Stability Data
Attix Pharmaceuticals is recalling Amoxicillin Trihydrate active pharmaceutical ingredient because stability data does not support the printed expiry dates.
Product
Amoxicillin Trihydrate active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1506-2015·2015-04-29
Specialty Appliance Works Recalls Universal Nuts for Incorrect Material Composition
Specialty Appliance Works is recalling Universal Nuts used in orthodontic Herbst Appliances because they were manufactured with 416 stainless steel instead of the specified 303 stainless steel.
Product
M-4 Mechanism Set 16 mm and M-4 Mechanism Set 19 mm A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1465-2015·2015-04-29
Biomet Recalls Lineum HF Torque Handle Limit Due to Component Updates
Biomet Spine is recalling 148 Lineum HF Torque Handle Limit units because the supplier withdrew the product for component updates or reconfiguration.
Product
Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct Usage: Designed to facilitate reconstruction of the cervical and upper thoracic spine using bones screws, locking plugs, and various types of rods, hooks, and lateral connectors.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-865-2015·2015-04-29
Attix Pharmaceuticals Recalls Procaine Penicillin G Due to Unverified Expiry Dates
Attix Pharmaceuticals is recalling Procaine Penicillin G active pharmaceutical ingredient because stability data does not support the printed expiry dates on repackaged lots.
Product
Procaine Penicillin G active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1507-2015·2015-04-29
Specialty Appliance Works Recalls Universal Nuts for Orthodontic Appliances
Specialty Appliance Works is recalling Universal Nuts for orthodontic Herbst Appliances because they were made with 416 stainless steel instead of the specified 303 stainless steel.
Product
HTM Mechanism Set Set 16, HTH Mechanism Set Size 18, HTH Mechanism Set Size 21 and HTH Mechanism Set Size 24 A Herbst Appliance is used to affect changes in the skeletal relationship and/or occlusion of a patient. the Universal Nut is a component of a Herbst Appliance.
Category
Medical Device
Distribution
Distributed nationwide