State

US Virgin Islands product recalls

73,388 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 39
Most recent: 2026-09-23

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21626–21650 of 73565

HighFDA (Devices)·Z-0660-2022·2022-03-02
Optima Coil System Recalled for Labeling and Packaging Mix-Up
BALT USA recalls Optima Coil System embolization devices due to labeling/pouch mix-up that could result in incorrect device selection during surgical procedures. Potential harms include vessel damage and aneurysm rupture.
Product
The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to a proximal stainless steel hypo-tube and distal body coil delivery pusher with a radiopaque distal positioning marker and proximal fluorosafe marker. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0667-2022·2022-03-02
Bard Surestep Intermittent Catheter Tray Recalled for Connection Leaks
C.R. Bard Inc recalled 1,620 units of Bard Surestep Intermittent Catheter Tray because the catheter may leak where it connects to the drain bag. No injuries have been reported.
Product
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0674-2022·2022-03-02
Comprehensive Shoulder System Mini Humeral Stem Recalled for Coating Adhesion Defect
Biomet recalls 11 units of its Comprehensive Shoulder System Mini Humeral Stem due to potential coating adhesion defects. An unvalidated rework process was applied to vendor-coated parts, risking implant failure.
Product
Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 11 MM, 83 MM Long Item Number: 113631
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22090·2022-03-02
ALDI Bee Happy Advent Calendars Recalled for Excessive Lead Paint
ALDI is recalling Bee Happy 12 Days of Craft Advent Calendars due to lead paint on a brown bell in Day 10 that exceeds the federal lead paint ban. The product poses a risk of lead poisoning if the paint is ingested, particularly for young children.
Product
Bee Happy 12 Days of Craft Advent Calendars
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0666-2022·2022-03-02
Bard SureStep Intermittent Catheter Tray recalled for potential leak defect
C.R. Bard is recalling 2,120 units of the BARD SURESTEP INTERMITTENT CATHETER TRAY (14Fr) due to a potential leak at the catheter-to-drain-bag connection.
Product
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0657-2022·2022-03-02
Medtronic Endurant Stent Graft Systems: Taper Tip Detachment Risk
Certain Medtronic Endurant stent graft systems may have taper tips that detach from the delivery system during implant procedures, potentially requiring secondary surgical intervention.
Product
Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF ENBF2313C120EE; ENBF2313C120EE; ENBF2313C145EE; ENBF2313C170EE; ENBF2316C120EE; ENBF2316C145EE; ENBF2316C170EE; ENBF2513C120EE; ENBF2513C145EE; ENBF2513C170EE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0675-2022·2022-03-02
Biomet Shoulder Implant Stem Coating Adhesion Defect Recall
Biomet is recalling shoulder implant stems due to improper rework of porous plasma coating, which may lack sufficient adhesion strength. Affected units may fail if the coating detaches.
Product
Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0626-2022·2022-03-02
Equate Nasal Spray Recalled for Contaminated Excipient Manufacturing Defect
Perrigo Company PLC is recalling Equate Nasal No Drip Nasal Spray because the product was manufactured with a contaminated excipient that was previously recalled from the supplier.
Product
EQUATE NASAL — EQUATE NASAL (OXYMETAZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0629-2022·2022-03-02
Perrigo Nasal Spray Recalled for Contaminated Excipient
Perrigo Company PLC is recalling NASAL Maximum Strength Nasal Spray (oxymetazoline HCl 0.05%) due to manufacturing with a contaminated excipient that was itself recalled from the supplier. The recall affects one batch distributed nationwide.
Product
NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0599-2022·2022-03-02
Equate Children's Pain and Fever recalled due to contaminated excipient
Perrigo Company is recalling Equate Children's Pain and Fever (Acetaminophen) oral suspension nationwide due to manufacturing deviations involving contaminated excipient from a supplier.
Product
EQUATE CHILDRENS PAIN AND FEVER — EQUATE CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0603-2022·2022-03-02
Basic Care No Drip Nasal Spray Recalled for Contaminated Excipient
Perrigo Company is recalling 37,104 bottles of Basic Care No Drip Nasal Spray (oxymetazoline hydrochloride 0.05%) nationwide due to contaminated excipient used during manufacturing. The affected batches were distributed to U.S. consumers.
Product
BASIC CARE NO DRIP NASAL — BASIC CARE NO DRIP NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0604-2022·2022-03-02
Perrigo Severe Congestion Nasal Spray recalled for contaminated excipient
Perrigo Company is recalling Severe Congestion Nasal Spray, No Drip Plus Menthol because the product was manufactured with a contaminated excipient that was recalled from the supplier.
Product
Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Packaged by Perrigo Company for: Big Lots Stores, Inc., P.O. Box 28523, Columbus, OH 43228-0523. NDC: 50594-719-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0570-2022·2022-03-02
Prevantics Maxi Swabstick Recall Due to Manufacturing Validation Issues
Professional Disposables International is recalling Prevantics Maxi Swabstick (chlorhexidine gluconate and isopropyl alcohol) due to unvalidated test methods used during manufacturing. The company has not reported any illnesses or injuries.
Product
PREVANTICS MAXI SWABSTICK — PREVANTICS MAXI SWABSTICK (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0600-2022·2022-03-02
Children's Acetaminophen Oral Suspension Recalled for Contaminated Excipient
Perrigo Company is recalling 561 bottles of Children's Pain & Fever Acetaminophen 160 mg per 5 mL oral suspension due to contamination from a recalled excipient ingredient used during manufacturing.
Product
Children's Pain & Fever Acetaminophen, 160 mg per 5 mL Oral Suspension combo pack. DS SR APAP 160MG CHLD BBGM/DF CHRY/GRP. UPC: 3 70030 11637 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0620-2022·2022-03-02
Oxymetazoline HCl Nasal Spray Recalled for Contaminated Excipient
Perrigo Company PLC is recalling NASAL Maximum Strength No Drip Nasal Spray (oxymetazoline HCl 0.05%) because the product was manufactured with a contaminated excipient from a recalled supplier.
Product
NASAL — NASAL (OXYMETAZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0572-2022·2022-03-02
Prevantics Swabstick Chlorhexidine Recall Due to Test Validation Uncertainty
Professional Disposables International is recalling Prevantics Swabstick (chlorhexidine gluconate and isopropyl alcohol) products nationwide due to uncertain validation of the test methods used during manufacturing.
Product
PREVANTICS SWABSTICK — PREVANTICS SWABSTICK (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0575-2022·2022-03-02
Dr. Reddy's Azacitidine Injectable Drug Recalled for Failed Stability
Dr. Reddy's Laboratories is recalling Azacitidine 100mg injectable vials nationwide due to failed stability specifications. Multiple lot numbers distributed across the United States are affected.
Product
AZACITIDINE — AZACITIDINE (AZACITIDINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0590-2022·2022-03-02
DG Health Children's Acetaminophen Recalled for Contaminated Excipient
Perrigo Company is recalling DG Health Children's Pain and Fever (acetaminophen) oral suspension because the product was manufactured with a contaminated excipient that was itself recalled by its supplier.
Product
DG HEALTH CHILDRENS PAIN AND FEVER — DG HEALTH CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0595-2022·2022-03-02
Infants Pain and Fever Acetaminophen recalled for contaminated excipient
Perrigo Company is recalling Infants Pain and Fever Acetaminophen Infant Dye Free Grape Oral Suspension due to contaminated excipient used in manufacturing. The recall affects 1,296 bottles distributed nationwide.
Product
INFANTS PAIN AND FEVER — INFANTS PAIN AND FEVER (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0587-2022·2022-03-02
Good Sense Acetaminophen Child Suspension Recalled Due to Contaminated Excipient
Perrigo is recalling Good Sense Pain and Fever acetaminophen child oral suspension (160mg/5ml, 4 FL OZ bottles) nationwide because the product was manufactured with a contaminated excipient that was recalled by the supplier.
Product
GOOD SENSE PAIN AND FEVER — GOOD SENSE PAIN AND FEVER (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0571-2022·2022-03-02
Prevantics Swab Drug Recall for Test Method Validation Deficiency
Professional Disposables International, Inc. is recalling Prevantics Swab (chlorhexidine gluconate and isopropyl alcohol) due to cGMP deviations involving inadequate validation of manufacturing test methods. The product was distributed nationwide in the USA and Puerto Rico.
Product
PREVANTICS SWAB — PREVANTICS SWAB (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0577-2022·2022-03-02
Bortezomib 3.5 mg Vials Recalled Due to Failed Stability Specifications
Dr. Reddy's Laboratories is recalling Bortezomib 3.5 mg single-dose vials nationwide due to failed stability specifications. Approximately 2,980 vials of lot H210233 (expiration 3/1/2023) are affected.
Product
Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-865-60
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0619-2022·2022-03-02
Perrigo Nasal Oxymetazoline Spray Recalled for Contaminated Excipient
Perrigo Company PLC is recalling approximately 10,800 bottles of NASAL Maximum Strength No Drip Nasal Spray (Oxymetazoline HCl 0.05%) nationwide due to manufacturing with a contaminated excipient supplied by their ingredient vendor.
Product
NASAL — NASAL (OXYMETAZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0611-2022·2022-03-02
Target Severe Congestion Nasal Spray recalled for contaminated excipient
Perrigo Company is recalling Target Severe Congestion Nasal Spray (Oxymetazoline HCl 0.05%) because it was manufactured with a contaminated excipient that had been recalled from the supplier.
Product
Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Dist. by Target Corp., Mpls., MN 55403. NDC 11673-935-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0606-2022·2022-03-02
DG Health Nasal Spray Recalled for Contaminated Excipient
Perrigo Company PLC is recalling DG Health Nasal Spray (Oxymetazoline HCl 0.05%) distributed nationwide because the product was manufactured with a contaminated excipient that was itself recalled from the supplier.
Product
DG HEALTH NASAL — DG HEALTH NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide