Class II · Moderate risk
Prevantics
cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.
National Drug Code
Is NDC 10819-4076-03 recalled?
Prevantics Maxi Swabstick · 300 POUCH in 1 CASE (10819-4076-3) / 5.1 mL in 1 POUCH
Yes — this exact package was recalled
1 FDA recall names the code 10819-4076-03 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- chlorhexidine gluconate and isopropyl alcohol
- Strength
- CHLORHEXIDINE GLUCONATE 31.5 mg/mL; ISOPROPYL ALCOHOL .7…
- Form
- Solution · Topical
- Labeler
- Professional Disposables International, Inc.
- Type
- Human OTC Drug
- Product code
- 10819-4076
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 10819-3891 See recall 3
- 10819-3883 PVP Iodine Prep Pad Medium and Large 2
- 10819-3885 PVP Iodine Prep Swabstick Ones and Threes 2
- 10819-1080 Prevantics Swab 1
- 10819-3890 See recall 1
- 10819-4077 Prevantics Swabstick 1
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