Prevantics (chlorhexidine gluconate and isopropyl alcohol) Maxi Swabstick, 3.15% w/v and 70% v/v, packaged as a) One Maxi Swabstick, 0.172 fl. Oz. (5.1 mL) Each in a pouch, 30 Individual Maxi Swabsticks per carton, 10 boxes of 30 Individual Swabsticks per case, NDC 10819-4076-4, REORDER NO. S41950; b) One Maxi Swabstick, 0.172 fl. Oz. (5.1 mL) Each in a pouch, 300 Individual Swabsticks per case, NDC 10819-4076-3, REORDER NO. S27350; Professional Disposables International, Inc., Orangeburg, NY 10962-1376.
Drug Recall
Official source record
- Recall number
- D-0570-2022
- Event ID
- 89547
- Classification
- Class II
- Status
- Terminated
- Recalling company
- Professional Disposables International, Inc.
- Reason for recall
- cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.
- Report date
- March 2, 2022
- Recall initiation date
- February 4, 2022
- Termination date
- October 31, 2023
- Distribution pattern
- Product was distributed nationwide in the USA and Puerto Rico.
Drug product identifiers
- Manufacturer
- Professional Disposables International, Inc.
- Brand name
- PREVANTICS MAXI SWABSTICK
- Generic name
- CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL
- Substance names
- CHLORHEXIDINE GLUCONATE; ISOPROPYL ALCOHOL
- Product NDC
- 10819-4076
- Package NDCs
- 10819-4076-3; 10819-4076-4
- Route
- TOPICAL
Where this information comes from
View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to the FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this medication?
Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.
Where can I find more official information?
The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.
