Class II · Moderate risk
PDI Povidone-Iodine Prep Pad Large
SubPotent: Out of Specification
National Drug Code
Is NDC 10819-3883-01 recalled?
PVP Iodine Prep Pad Medium and Large · 100 PACKET in 1 BOX (10819-3883-1) / .8 mL in 1 PACKET
Yes — this exact package was recalled
1 FDA recall names the code 10819-3883-01 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
- providone iodine
- Strength
- POVIDONE-IODINE 10 mg/mL
- Form
- Swab · Topical
- Labeler
- Professional Disposables International, Inc.
- Type
- Human OTC Drug
- Product code
- 10819-3883
Recalls naming this package
Class II · Moderate risk
PDI Povidone-Iodine Prep Pad MEDIUM
SubPotent: Out of Specification
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
- 10819-3885 PVP Iodine Prep Swabstick Ones and Threes 2
- 10819-1080 Prevantics Swab 1
- 10819-3890 See recall 1
- 10819-4076 Prevantics Maxi Swabstick 1
- 10819-4077 Prevantics Swabstick 1
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