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.

43201–43225 of 73919

ModerateFDA (Devices)·Z-2159-2017·2017-05-31
MesaLabs Conductivity Standard Solution Recalled for Specification Failure
Mesa Laboratories is recalling 9,900 units of Conductivity/TDS Calibrator Solution because the product failed to meet specifications. The solution is used for calibrating hemodialysis equipment and does not contact patients.
Product
MesaLabs Conductivity Standard Solution, 14 mS/cm, 32 ounces (950 ml). Product No. : 02.0027, 020510 (carton of 6 of 02.0027). Polyethylene bottle Conductivity/TDS Calibrator solutions are a secondary standard solution used for the calibration of conductivity/TDS cells…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0823-2017·2017-05-31
Advanced Pharma Recalls 0.9% Sodium Chloride Slip Tip for Latex Labeling
Advanced Pharma Inc. is recalling 0.9% Sodium Chloride Slip Tip products because they may contain latex without proper labeling.
Product
0.9% Sodium Chloride Slip Tip all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0822-2017·2017-05-31
Advanced Pharma Recalls Heparin Sodium Due to Latex Labeling
Advanced Pharma Inc. is recalling all strengths and dosage forms of Heparin sodium because the product may contain synthetic or natural latex without proper labeling.
Product
Heparin sodium all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0850-2017·2017-05-31
Advanced Pharma Recalls Sodium Phosphate for Latex Labeling Defect
Advanced Pharma Inc. is recalling Sodium Phosphate products because they may contain latex but lack proper labeling. The recall covers all strengths and dosage forms distributed nationwide.
Product
Sodium Phosphate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2126-2017·2017-05-31
BioMerieux Recalls Ceftriaxone ETEST Kits Due to Performance Issues
BioMerieux SA is recalling Ceftriaxone ETEST kits due to a potential performance issue affecting strain categorization.
Product
Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic ba
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0829-2017·2017-05-31
Advanced Pharma Recalls Calcium Gluconate for Latex Labeling Deficiency
Advanced Pharma Inc. is recalling Calcium Gluconate products because they may contain latex without proper labeling.
Product
Calcium Gluconate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0851-2017·2017-05-31
Advanced Pharma Recalls Sodium Citrate Due to Latex Labeling Defect
Advanced Pharma Inc. is recalling all strengths and dosage forms of Sodium Citrate because the product may contain latex without proper labeling.
Product
Sodium Citrate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2156-2017·2017-05-31
Siemens AXIOM Sensis Diagnostic Computer Recalled for Dust-Related Failures
Siemens Medical Solutions is recalling 4,095 AXIOM Sensis diagnostic computers because dust accumulation can cause system failures, potentially interrupting clinical treatments.
Product
AXIOM Sensis, Computer, Diagnostic, Programmable. Intended to be used as a diagnostic and administrative tool supporting hemodynamic cardiac catheterizations and/or intracardiac electrophysiology studies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0849-2017·2017-05-31
Advanced Pharma Recalls Potassium Phosphate Due to Latex Labeling Defect
Advanced Pharma Inc. is recalling all strengths and dosage forms of Potassium Phosphate because the product may contain latex but lacks proper labeling.
Product
Potassium Phosphate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0847-2017·2017-05-31
Advanced Pharma Recalls Cardioplegic Solution for Latex Labeling Defect
Advanced Pharma Inc. is recalling Cardioplegic Solution Maintenance due to a labeling error regarding potential latex content.
Product
Cardioplegic Solution Maintenance all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0814-2017·2017-05-31
Advanced Pharma Recalls Midazolam HCl for Potential Latex Content
Advanced Pharma Inc. is recalling all lots of Midazolam HCl because the product may contain synthetic or natural latex.
Product
Midazolam HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0813-2017·2017-05-31
Advanced Pharma Recalls Ketamine HCl for Potential Latex Content
Advanced Pharma Inc. is recalling all lots of Ketamine HCl because the product may contain synthetic or natural latex.
Product
Ketamine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0831-2017·2017-05-31
Advanced Pharma Recalls Succinylcholine Chloride for Latex Labeling Defect
Advanced Pharma Inc. is recalling all lots of Succinylcholine Chloride because the product may contain latex but lacks proper labeling.
Product
Succinylcholine Chloride all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0826-2017·2017-05-31
Advanced Pharma Recalls Ephedrine Sulfate Due to Latex Labeling Defect
Advanced Pharma Inc. is recalling all lots of Ephedrine Sulfate because the product may contain latex but lacks proper labeling.
Product
Ephedrine Sulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0812-2017·2017-05-31
Advanced Pharma Recalls Morphine Sulfate for Latex Labeling Deficiency
Advanced Pharma Inc. is recalling all lots of Morphine Sulfate because the product labeling does not indicate that it may contain synthetic or natural latex.
Product
Morphine Sulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0835-2017·2017-05-31
Advanced Pharma Recalls Rocuronium Bromide Due to Latex Labeling
Advanced Pharma Inc. is recalling all strengths and forms of Rocuronium Bromide because the product may contain latex without proper labeling.
Product
Rocuronium Bromide all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0832-2017·2017-05-31
Advanced Pharma Recalls Adenosine Due to Latex Labeling Deficiency
Advanced Pharma Inc. is recalling all lots of Adenosine because the product may contain latex but lacks appropriate labeling.
Product
Adenosine all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0860-2017·2017-05-31
Mylan Recalls Tarina Fe 1/20 Tablets Due to Chemical Contamination
Mylan Pharmaceuticals is recalling Tarina Fe 1/20 tablets due to chemical contamination from paint thinner vapors during manufacturing.
Product
Tarina Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets, USP and Ferrous Fumarate Tablets), 1 blister pack containing 28 tablets (NDC 50102-128-01), packaged in 3 pouches, each pouch contains one blister pack of 28 tablets (NDC 50102-128-03), Rx only, Manufactured…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2120-2017·2017-05-31
Bard StatLock IV Premium Catheter Stabilization Device Recalled for Sizing Error
Bard Access Systems is recalling 4,500 units of StatLock IV Premium Catheter Stabilization Devices because they may contain incorrectly sized retainer clips.
Product
StatLock¿ IV Premium Catheter Stabilization Device, product code IV0570. sterile. Packaging: packaged as single units in tyvek to film pouches, the product is distributed in cartons containing 25 devices and cases containing 250 devices.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2124-2017·2017-05-31
Beckman Coulter Recalls Microalbumin Reagent Due to Potential Out-of-Range Recovery
Beckman Coulter is recalling Microalbumin Reagent Lot M609458 because it may recover outside the lower limit of the published insert range for Urine Protein Control Level 1.
Product
Microalbumin Reagent, Catalog No. 475100, Product Labeling A18520AL MA reagent, when used in conjunction with UniCel DxC 600/800 System(s) and SYNCHRON¿ Systems MA Calibrator, is intended for quantitative determination of Albumin concentration in human urine
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0840-2017·2017-05-31
Advanced Pharma Recalls Atropine Sulfate for Latex Labeling Defect
Advanced Pharma Inc. is recalling all lots of Atropine Sulfate because the product may contain latex but lacks appropriate labeling.
Product
Atropine Sulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2017·2017-05-31
Advanced Pharma Recalls Esmolol HCl Due to Latex Labeling Defect
Advanced Pharma Inc. is recalling all Esmolol HCl products because the labeling does not indicate that the products may contain synthetic or natural latex.
Product
Esmolol HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
LowFDA (Food)·F-2250-2017·2017-05-31
Schiff Move Free Advanced Tablets Recalled for Incorrect Packaging
RB Manufacturing is recalling Schiff Move Free Advanced Plus MSM & Vitamin D3 tablets due to incorrect packaging.
Product
Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-11873
Category
Food
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0857-2017·2017-05-31
Sun Pharmaceutical Recalls Children's Cetirizine Tablets for Hardness Issues
Sun Pharmaceutical Industries is recalling 13,200 bottles of Children's Cetirizine Hydrochloride Chewable Tablets due to out-of-specification tablet hardness.
Product
Children's Cetirizine Hydrochloride Chewable Tablets, 5 mg, 30-count bottle, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol - 389 350, Gujarat, India; Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 47335-343-83.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2121-2017·2017-05-31
Medtest Recalls Pointe Scientific Chemistry Controls Due to Mean Assignment Error
Medtest Holdings is recalling Pointe Scientific Chemistry Controls Level I and II because the original mean assigned to the controls was too high, resulting in a new assigned mean outside the published range.
Product
Pointe Scientific Chemistry Controls Level I and II LEVl: Amber glass vial w/PP white plastic cap. LEV2: Amber glass vial w/PP black plastic cap.
Category
Medical Device
Distribution
Distributed nationwide