State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36526–36550 of 73915

ModerateFDA (Drugs)·D-0067-2019·2018-10-24
Rite Aid First Aid Antibiotic Ointment Recalled for Low Bacitracin Zinc
Product Quest Manufacturing LLC is recalling Rite Aid First Aid Antibiotic Ointment because the bacitracin zinc ingredient was found to be subpotent.
Product
Rite Aid Pharmacy, First Aid Antibiotic Ointment, (neomycin sulfate 3.5 mg, polymyxin B sulfate 5,000 units, bacitracin zinc 400 units per gram), 2 OZ (56 g) tube, Distributed By: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011, UPC 0 11822 55441 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0068-2019·2018-10-24
FDA Recalls Premier Value Muscle Rub Due to High Menthol Levels
Product Quest Manufacturing LLC is recalling Premier Value Fast Relief Muscle Rub because the menthol ingredient exceeded specification limits.
Product
Premier Value, Fast Relief, Muscle Rub, (menthol 10% and methyl salicylate 15%) 4 OZ (113 g) tube, Distributed By: Chain Drug Consortium, 3301 NW Boca Raton Blvd., Suite 101, Boca Raton, FL, 33431, UPC 8 40986 01341
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0060-2019·2018-10-24
Walgreens Nasal Decongestant Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Walgreens Nasal Spray (Oxymetazoline HCl 0.05%) due to CGMP deviations that could impact product quality.
Product
Walgreens, Nasal Spray (Oxymetazoline HCl 0.05%) Nasal Decongestant, Maximum Strength, 12 Hour, 0.75 FL OZ (22 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015, UPC 3 11917 18622 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0182-2019·2018-10-24
OriGen Dual Lumen Cannula Recalled for Manufacturing Deficiencies
OriGen Biomedical is recalling 169 units of Reinforced Dual Lumen Cannulas due to missing barium sulfate and inaccurate tip length markings.
Product
Reinforced Dual Lumen Cannula, 23Fr., REF: VV23F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0140-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect
Zimmer Biomet is recalling 22 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.
Product
Affixus Hip Fracture Nail Right 125 13 mm x 280 mm, Item Number 814313280 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0162-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 20 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.
Product
Affixus Hip Fracture Nail Right 130 11 mm x 400 mm, Item Number 814511400 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0124-2019·2018-10-24
Affixus Hip Fracture Nails Recalled Due to Compromised Sterile Packaging
The FDA is recalling 72 Affixus Hip Fracture Nails because sterile packaging was found open during surgery, creating a potential contamination risk.
Product
Affixus Hip Fracture Nail Right 125 9 mm x 300 mm, Item Number 814309300 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0189-2019·2018-10-24
Siemens Recalls Atellica Sample Handler Prime Software Due to Behavioral Issues
Siemens Healthcare Diagnostics is recalling Atellica Sample Handler Prime software versions 1.13 and lower due to five identified behavioral issues affecting diagnostic testing.
Product
Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is a multi-component system for in vitro diagnostic testing of clinical specimens.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0161-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 44 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers US and foreign distribution.
Product
Affixus Hip Fracture Nail Right 130 11 mm x 360 mm, Item Number 814511360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0127-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 24 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.
Product
Affixus Hip Fracture Nail Right 125 9 mm x 360 mm, Item Number 814309360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0073-2019·2018-10-24
CVS Triple Antibiotic Ointment Spray Recalled for Low Bacitracin Zinc Levels
Product Quest Manufacturing LLC is recalling CVS Health Triple Antibiotic Ointment Spray because the bacitracin zinc ingredient was found to be subpotent.
Product
CVS Health, Original Strength, Triple Antibiotic Ointment Spray (bacitracin zinc 400 units, neomycin sulfate 3.5 mg, polymyxin B sulfate 5,000 units per gram), 2 OZ (57 g) can, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, Product#957603, UPC 0 50428…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0036-2019·2018-10-24
Saline Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Discount Drug Mart and Food Fair Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Discount Drug Mart, Food Fair, Saline Nasal Spray (sodium chloride) 0.65%, packaged as a) 3 FL OZ (89 mL) bottle UPC 0 93351 01833 6; b) 1.5 FL OZ (45 mL) bottle UPC 0 93351 01834 3, Distributed by: Discount Drug Mart, 211 Commerce Drive, Medina, OH 44256
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0172-2019·2018-10-24
Life Technologies Recalls Gibco DPBS Due to Leaky Bottle Caps
Life Technologies is recalling 240 units of Gibco DPBS due to defective bottle caps that compromise sterility.
Product
Gibco DPBS, calcium, magnesium, for In-Vitro Diagnostic Use SKU 14040141
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0032-2019·2018-10-24
CVS Health Sterile Saline Nasal Mist Recalled for Quality Deviations
Product Quest Manufacturing LLC is recalling CVS Health Sterile Saline Nasal Mist due to manufacturing deviations that could impact product quality.
Product
CVS Health, Sterile Saline Nasal Mist (sodium chloride) Allergy & Sinus Relief, 3.0%, 4.25 OZ (126 g) can, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 41854 3.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0123-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defect
Zimmer Biomet is recalling 24 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the product was opened in surgery.
Product
Affixus Hip Fracture Nail Right 125 9 mm x 260 mm, Item Number 814309260 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0115-2019·2018-10-24
Siemens ADVIA Centaur CKMB Master Curve Material Recalled for Bias
Siemens Healthcare Diagnostics is recalling ADVIA Centaur CKMB Master Curve Material due to a potential bias identified when compared to internal standards.
Product
ADVIA Centaur CKMB Master Curve Material, Cat No. 07867768 Product Usage: For in vitro diagnostic use for evaluating the ADVIA Centaur CKMB assay. This material is intended to be run singly as unknown samples after a two-point calibration has been performed on the system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0146-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 78 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.
Product
Affixus Hip Fracture Nail Left 125 9 mm x 300 mm, Item Number 814409300 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0153-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Defects
Zimmer Biomet is recalling 68 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and two foreign countries.
Product
Affixus Hip Fracture Nail Left 125 11 mm x 360 mm, Item Number 814411360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0055-2019·2018-10-24
Product Quest Recalls OCEAN Saline Nasal Spray Due to Quality Deviations
Product Quest Manufacturing LLC is recalling OCEAN Saline Nasal Spray bottles nationwide because they were manufactured under conditions that could impact product quality.
Product
OCEAN Saline Nasal Spray, packaged in a) 3.5 Fl. Oz. (104 mL) bottle UPC 3 01875 26001 9; b) 45 cc (1.5 fl. oz.) UPC 3 01875 26003 3, c) Buddy Pack containing one 1.5 FL. OZ. (44 mL) and one 0.76 FL.OZ. (22 mL) bottle per carton, Distributed by: Valeant Consumer Products, A…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0080-2019·2018-10-24
Product Quest Recalls Family Dollar Saline Nasal Spray for Quality Issues
Product Quest Manufacturing LLC is recalling Family Dollar Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Family Dollar Saline Nasal Spray 4.25 oz. can, 24 pk, SKU 0900562.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0121-2019·2018-10-24
CryoLife Pulmonary Hemi-Artery Graft Recalled for Labeling Error
CryoLife, Inc. is recalling one CryoPatch SG Pulmonary Hemi-Artery graft because the conduit and branch lengths were switched on the product labeling.
Product
CryoPatch SG Pulmonary Hemi-Artery, 1 graft
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0078-2019·2018-10-24
Rexall Nasal Spray Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Rexall Extra Moisturizing No Drip Nasal Spray due to manufacturing conditions that could impact product quality.
Product
Rexall, Extra Moisturizing No Drip Nasal Spray (Oxymetazoline Hydrochloride 0.05%) 1 FL OZ (30 mL) bottle, 48 pk. (12687901)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0054-2019·2018-10-24
TopCare Saline Nasal Gel Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling TopCare Saline Nasal Gel with Soothing Aloe due to manufacturing conditions that could impact product quality.
Product
TopCare, Saline Nasal Gel with Soothing Aloe, 0.5 OZ (14 g) tube, Distributed By Topco Associates LLC, Elk Grove Village, IL 60007, UPC 0 36800 42146 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0163-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 50 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the products were opened in surgery.
Product
Affixus Hip Fracture Nail Right 130 13 mm x 360 mm, Item Number 814513360 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0130-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 20 Affixus Hip Fracture Nails because complaints indicated the sterile packaging was already open when the product was opened in surgery.
Product
Affixus Hip Fracture Nail Right 125 9 mm x 460 mm, Item Number 814311460 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide