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Class II: temporary or reversible health riskTerminated

Professional Disposables International Prevantics Recall

Prevantics (chlorhexidine gluconate and isopropyl alcohol) Maxi Swabstick, 3

Professional Disposables International, Inc. · Orangeburg, NY

Risk level
Class II
Reported by FDA
Mar 2, 2022
Recall ID
D-0570-2022
Check your lot numberHow we source this data

Summary

Professional Disposables International recalled Prevantics starting Feb 4, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0570-2022 on Mar 2, 2022. Reason: cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products. Status: Terminated.

Why it was recalled

cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.

Product description

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.

Lot numbers, UPCs & expiration codes

Lot #: a) 12000315, Exp Feb 2022; 12000700, Exp Mar 2022; 12001112 LE, Exp Jun 2022; 12001214, Exp Jul 2022; 12001362, 12001406, Exp Aug 2022; 12001628, Exp Sep 2022; 12001856, Exp Oct 2022; 12002103, Exp Dec 2022; 12002113, 12100024, Exp Jan 2023; 12100226, 12100227, Exp Feb 2023; 12100443, 12100503, Exp Mar 2023; 12100516, 12100517, Exp Apr 2023; 12100748, 12100756, Exp May 2023; b) 12001113 LE, Exp Jun 2022; 12001289, 12001240, Exp Jul 2022; 12002104, Exp Dec 2022; 12100025, Exp Jan 2023; 12100405, Exp Mar 2023; 12100674, Exp Apr 2023; 12100779, Exp May 2023

Where it was sold

Product was distributed nationwide in the USA and Puerto Rico.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0570-2022
Classification
Class II
Status
Terminated
Recall initiated
Feb 4, 2022
FDA report date
Mar 2, 2022
Quantity
a) 9518 cases; b) 3347 cases
Recall type
Voluntary: Firm initiated
Recalling firm
Professional Disposables International, Inc.

Original FDA data

Every field from FDA enforcement report D-0570-2022, exactly as published.

Show all FDA fields
City
Orangeburg
State
NY
Status
Terminated
Country
United States
Event ID
89547
Address
2 Nice Pak Park
Code information
Lot #: a) 12000315, Exp Feb 2022; 12000700, Exp Mar 2022; 12001112 LE, Exp Jun 2022; 12001214, Exp Jul 2022; 12001362, 12001406, Exp Aug 2022; 12001628, Exp Sep 2022; 12001856, Exp Oct 2022; 12002103, Exp Dec 2022; 12002113, 12100024, Exp Jan 2023; 12100226, 12100227, Exp Feb 2023; 12100443, 12100503, Exp Mar 2023; 12100516, 12100517, Exp Apr 2023; 12100748, 12100756, Exp May 2023; b) 12001113 LE, Exp Jun 2022; 12001289, 12001240, Exp Jul 2022; 12002104, Exp Dec 2022; 12100025, Exp Jan 2023; 12100405, Exp Mar 2023; 12100674, Exp Apr 2023; 12100779, Exp May 2023
Postal code
10962-1317
Report date
Mar 2, 2022
Product type
Drugs
Recall number
D-0570-2022
Classification
Class II
Recalling firm
Professional Disposables International, Inc.
Product quantity
a) 9518 cases; b) 3347 cases
Termination date
Oct 31, 2023
Reason for recall
cGMP deviations: uncertainty of the adequacy of the validation of the test methods used to manufacture the products.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
Distribution pattern
Product was distributed nationwide in the USA and Puerto Rico.
Recall initiation date
Feb 4, 2022
Initial firm notification
Letter
Center classification date
Feb 18, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0570-2022, published Mar 2, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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