Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported March 2, 2022
Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick, 3.15% w/v and 70% v/v, packaged as a) One Swabstick, 0.054 fl. oz. (1.6 mL) Each in a pouch, NDC 10819-4077-1; 50 Individual Swabsticks per carton, 10 boxes of 50 Individual Swabsticks per case, REORDER NO. S40750, NDC 10819-4077-4; b) One Swabstick, 0.054 fl. Oz. (1.6 mL) Each in a pouch, 500 Individual Swabsticks per case, REORDER NO. S32450, NDC 10819-4077-2; c) One Swabstick, 0.054 fl. Oz. (1.6 mL) Each in a pouch, 500 Ind
cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.
Professional Disposables International, Inc. recalled Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick, 3.15% w/v and 70% v… - a moderate-severity action.
Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick, 3.15% w/v and 70% v… was recalled by Professional Disposables International, Inc. in March 2, 2022. Reason: cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the pr…. Check the official notice for the remedy. Verify recall #D-0572-2022 with the FDA Drug before acting.
The recall
Professional Disposables International, Inc. issued this moderate-severity FDA Drug recall-cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the pr….
- Moderate
- severity level
- Class II
- classification
- March 2, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0572-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0572-2022) was formally reported on March 2, 2022, with the manufacturer initiating the action on February 4, 2022. It is classified under Moderate severity (Class II), with a current status of Terminated. Professional Disposables International, Inc. is listed as the recalling firm, operating out of Orangeburg, NY. Federal records list the affected scope as a) 28201 cases; b) 7579 cases; c) 8882 cases.
The documented reason for this recall is: cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products. Distribution data in the federal record shows the product reached: Product was distributed nationwide in the USA and Puerto Rico.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
a) 28201 cases; b) 7579 cases; c) 8882 cases
Related Recalls
6
5 from same agency
Product description
Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick, 3.15% w/v and 70% v/v, packaged as a) One Swabstick, 0.054 fl. oz. (1.6 mL) Each in a pouch, NDC 10819-4077-1; 50 Individual Swabsticks per carton, 10 boxes of 50 Individual Swabsticks per case, REORDER NO. S40750, NDC 10819-4077-4; b) One Swabstick, 0.054 fl. Oz. (1.6 mL) Each in a pouch, 500 Individual Swabsticks per case, REORDER NO. S32450, NDC 10819-4077-2; c) One Swabstick, 0.054 fl. Oz. (1.6 mL) Each in a pouch, 500 Individual Swabsticks per case, REORDER NO. S42850, NDC 10819-4077-3; Professional Disposables International, Inc., Orangeburg, NY 10962-1376.
Reason for recall
cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0572-2022 |
| Date reported | March 2, 2022 |
| Date initiated | February 4, 2022 |
| Recalling firm | Professional Disposables International, Inc. |
| Firm location | Orangeburg, NY |
| Affected scope | a) 28201 cases; b) 7579 cases; c) 8882 cases |
| Distribution | Product was distributed nationwide in the USA and Puerto Rico. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0572-2022) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick, 3.15% w/v and 70% v/v, packaged as a) One Swabstick, 0.054 fl. oz. (1.6 mL) Each in a pouch, NDC 10819-4077-1; 50 Individual Swabsticks per carton, 10 boxes of 50 Individual Swabsticks per case, REORDER NO. S40750, NDC 10819-4077-4; b) One Swabstick, 0.054 fl. Oz. (1.6 mL) Each in a pouch, 500 Individual Swabsticks per case, REORDER NO. S32450, NDC 10819-4077-2; c) One Swabstick, 0.054 fl. Oz. (1.6 mL) Each in a pouch, 500 Individual Swabsticks per case, REORDER NO. S42850, NDC 10819-4077-3; Professional Disposables International, Inc., Orangeburg, NY 10962-1376.. Recalled by Professional Disposables International, Inc.. Units affected: a) 28201 cases; b) 7579 cases; c) 8882 cases.
Why was this product recalled? ▼
cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 2, 2022. Severity: Moderate. Recall number: D-0572-2022.
Where was the recalled product distributed? ▼
Distribution: Product was distributed nationwide in the USA and Puerto Rico..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0572-2022) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported March 2, 2022. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.