Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swab, 3.15% w/v and 70% v/v, packaged as a) One Swab, 0.034 fl. Oz. (1 mL) Each in a pouch, 100 Individual Swabs per carton, 10 boxes of 100 Individual Swabs per case, REORDER NO. B10800, NDC 10819-1080-1; b) One Swab, 0.034 fl. oz. (1 mL) Each in a pouch, 3000 Individual Swabs per case, REORDER NO. B11400, NDC 10819-1080-2; Professional Disposables International, Inc., Orangeburg, NY 10962-1376.
Reported: March 2, 2022 Initiated: February 4, 2022 #D-0571-2022
Product Description
Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swab, 3.15% w/v and 70% v/v, packaged as a) One Swab, 0.034 fl. Oz. (1 mL) Each in a pouch, 100 Individual Swabs per carton, 10 boxes of 100 Individual Swabs per case, REORDER NO. B10800, NDC 10819-1080-1; b) One Swab, 0.034 fl. oz. (1 mL) Each in a pouch, 3000 Individual Swabs per case, REORDER NO. B11400, NDC 10819-1080-2; 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.
Details
- Recalling Firm
- Professional Disposables International, Inc.
- Units Affected
- a) 160531 cases; b) 16123 cases
- Distribution
- Product was distributed nationwide in the USA and Puerto Rico.
- Location
- Orangeburg, NY
Frequently Asked Questions
What product was recalled? ▼
Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swab, 3.15% w/v and 70% v/v, packaged as a) One Swab, 0.034 fl. Oz. (1 mL) Each in a pouch, 100 Individual Swabs per carton, 10 boxes of 100 Individual Swabs per case, REORDER NO. B10800, NDC 10819-1080-1; b) One Swab, 0.034 fl. oz. (1 mL) Each in a pouch, 3000 Individual Swabs per case, REORDER NO. B11400, NDC 10819-1080-2; Professional Disposables International, Inc., Orangeburg, NY 10962-1376.. Recalled by Professional Disposables International, Inc.. Units affected: a) 160531 cases; b) 16123 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-0571-2022.
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