State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39876–39900 of 73919

ModerateFDA (Devices)·Z-0550-2018·2018-02-14
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling 10,116 units of Natural Nail System Tear Drop Guide Wires because the previous packaging configuration lacked design verification for 70cm wires.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length, Item Number 47-2490-098-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0338-2018·2018-02-14
McKesson Recalls Subpotent Megestrol Acetate Oral Suspension
McKesson Packaging Services is recalling Megestrol Acetate Oral Suspension because stability testing found the drug was subpotent.
Product
Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups), Rx Only, Dist. By McKesson Packaging Services a business unit of McKesson Corporation 7101 Weddington Rd. Concord, NC 28027, NDC 63739-549-51
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0548-2018·2018-02-14
Astellas Recalls Mycamine Injection Vials Due to Labeling Error
Astellas Pharma US Inc is recalling 63,600 vials of Mycamine (micafungin sodium) for Injection due to a label error on the declared strength.
Product
MYCAMINE — MYCAMINE (MICAFUNGIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0529-2018·2018-02-14
Angiodynamics Recalls Accu2i pMTA Microwave Tissue Ablation Applicators
Angiodynamics is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering the desired microwave energy.
Product
Accu2i pMTA Applicator, 14 cm STANDARD, REF/Catalog # 900-600-US, Model # (UPN) H787900600US0, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0551-2018·2018-02-14
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling 1,631 units of Natural Nail System Tear Drop Guide Wires because the previous packaging configuration lacked design verification for 70cm wires.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 70 cm length, Item Number 47-2490-098-01 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0325-2018·2018-02-14
Flawless Beauty Recalls Relumins Vitamin C Ampules for Misbranding
Flawless Beauty LLC is voluntarily recalling all lots of Relumins Vitamin C Solvent ampules because they were marketed without an approved NDA or ANDA.
Product
Relumins Vitamin C Solvent ampules
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0327-2018·2018-02-14
Flawless Beauty Recalls Laroscorbine Platinum Vitamin C Due to Misbranding
Flawless Beauty LLC is voluntarily recalling all lots of Laroscorbine Platinum Vitamin C products because they were marketed without an approved NDA or ANDA.
Product
Laroscorbine Platinum Vitamin C 1 gm Collagen 0.35 gm, Roche
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0542-2018·2018-02-14
Busse Lumbar Puncture Tray Recalled for Foreign Matter
Busse Hospital Disposables is recalling Safety-Deluxe Lumbar Puncture Trays because they may contain loose polypropylene foreign matter above release specifications.
Product
Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0537-2018·2018-02-14
Medtronic Ascenda Intrathecal Catheter Recall for Kinking Risk
Medtronic is recalling specific lots of Ascenda Intrathecal Catheters due to a potential risk of kinking at the proximal end where the catheter connects to the drug infusion pump.
Product
Medtronic Ascenda(R) Intrathecal Catheter, Models: (a) 8780, UDI: 00643169202122, 00643169783027 (b) 8781, UDI: 00643169202139 (c) 8784, UDI: 00643169202153 The Ascenda Intrathecal Catheter kits (models 8780, 8781 and 8784) contain parts of an infusion system that…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0545-2018·2018-02-14
Busse Lumbar Puncture Tray Recalled for Foreign Matter
Busse Hospital Disposables is recalling Lumbar Puncture Trays because they may contain loose polypropylene foreign matter above release specifications.
Product
Lumbar Puncture Tray, Catalog # 1862 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0547-2018·2018-02-14
Zimmer Biomet Recalls Humeral Guide Wires Due to Packaging Design Verification
Zimmer Biomet is recalling 6,290 units of M/DN Intramedullary Fixation Humeral Guide Wires because the previous packaging configuration lacked design verification for 70cm wires.
Product
M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only, Item Number 00-2255-025-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0544-2018·2018-02-14
Busse Laceration Tray Recall Due to Foreign Matter
Busse Hospital Disposables is recalling Laceration Trays because they may contain loose polypropylene foreign matter above release specifications.
Product
Laceration Tray, Catalog # 1892R1 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0540-2018·2018-02-14
Busse Lumbar Puncture Tray Recalled for Foreign Matter
Busse Hospital Disposables is recalling Safety-Deluxe Lumbar Puncture Trays because they may contain loose polypropylene foreign matter above release specifications.
Product
Safety-Deluxe Lumbar Puncture Tray, Catalog # 974 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0524-2018·2018-02-14
Siemens Syngo.plaza PACS Software Recall for Workflow Display Error
Siemens is recalling 76 Syngo.plaza systems with SW VB20A because prior studies may not replace correctly in all workflow steps, potentially showing outdated images.
Product
Syngo.plaza systems with SW VB20A, Model Number - 10863171, 10863172, 10863173 Product Usage: Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0546-2018·2018-02-14
Busse Bone Marrow Biopsy Tray Recalled for Foreign Matter
Busse Hospital Disposables is recalling Safety Deluxe Bone Marrow Biopsy/Aspiration Trays because they may contain loose polypropylene foreign matter.
Product
Safety Deluxe Bone Marrow Biopsy/Aspiration Tray, Catalog # 986 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0540-2018·2018-02-14
Teva Recalls Fentanyl Transdermal Systems Due to Impurity Exceeding Limits
Teva Pharmaceuticals USA is recalling Fentanyl Transdermal Systems 25 mcg/h because a degradation product exceeded specification limits.
Product
Fentanyl Transdermal System. 25 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3198-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3198-54.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0425-2018·2018-02-14
Millennium Pharmaceuticals Recalls VELCADE Injection Vials Due to Defective Crimps
Millennium Pharmaceuticals is recalling 154,372 vials of VELCADE (bortezomib) for injection due to confirmed reports of loose vial crimps.
Product
VELCADE (bortezomib) for injection, 3.5 mg/vial, Reconstitution Information, SUBCUTANEOUS INJECTION ONLY add 1.4 mL 0.9% Sodium Chloride to make 2.5 mg/ mL final concentration, INTRAVENOUS INJECTION ONLY add 3.5 mL Sodium Chloride to 1 mg/mL final concentration, Rx Only…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0541-2018·2018-02-14
Busse Safety-Deluxe Biopsy Tray Recalled for Foreign Matter
Robert Busse & Co. is recalling Safety-Deluxe Basic Soft Tissue Biopsy Trays because they may contain loose polypropylene foreign matter.
Product
Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle, Catalog # 977 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0542-2018·2018-02-14
Teva Recalls Fentanyl Transdermal Systems Due to Impurity Levels
Teva Pharmaceuticals is recalling specific lots of Fentanyl Transdermal Systems because they contain a degradant called Fentanyl-n-Oxide that exceeds safety limits.
Product
Fentanyl Transdermal System. 75 mcg/h, packaged in 5 pouch system (NDC 0591-3213-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3213-54.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0809-2018·2018-02-14
Bobo's Coconut Oat Bars Recalled Due to Mold Contamination
Simply Delicious, Inc. is recalling Bobo's Coconut Oat Bars because they may contain mold. The recall covers 588 master cases distributed nationwide.
Product
Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per single bar
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0526-2018·2018-02-14
Angiodynamics Recalls Accu2i pMTA Microwave Tissue Ablation Applicators
Angiodynamics, Inc. is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering desired microwave energy.
Product
Accu2i pMTA Applicator, 14 cm STANDARD, REF/Catalog # 900-600, Model # (UPN) H7879006000, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the intraoperative…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0549-2018·2018-02-14
Zimmer Biomet Recalls Humeral Guide Wire Ball Tip Due to Packaging Design Verification
Zimmer Biomet is recalling 7,888 Humeral Guide Wire Ball Tip units because the previous packaging configuration lacks design verification for 70cm wires.
Product
Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length, Item Number 47-2255-008-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during implantation. The guide…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0250-2018·2018-02-14
G & W Laboratories Recalls Ciclopirox Olamine Cream Due to Discoloration
G & W Laboratories is recalling 142,236 tubes of Ciclopirox Olamine Cream USP, 0.77%, due to yellow discoloration. The product is distributed nationwide and in Puerto Rico.
Product
CICLOPIROX OLAMINE — CICLOPIROX OLAMINE (CICLOPIROX OLAMINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0541-2018·2018-02-14
Teva Recalls Fentanyl Patches Due to Impurity Exceeding Limits
Teva Pharmaceuticals is recalling Fentanyl Transdermal Systems because a degradation product exceeded safety limits.
Product
Fentanyl Transdermal System, 50 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3212-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3212-54.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0543-2018·2018-02-14
Teva Recalls Fentanyl Transdermal Systems Due to Impurity Exceeding Limits
Teva Pharmaceuticals is recalling specific lots of Fentanyl Transdermal Systems because a degradation product exceeded safety limits.
Product
Fentanyl Transdermal System, 100 mcg/h, packaged in 5 pouch system (NDC 0591-3214-72), Rx Only, Manufactured by: Actavis Laboratoies UT, Inc. Salt Lake City, UT 84108, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA. Individual pouch NDC 0591-3214-54.
Category
Drug
Distribution
Distributed nationwide