PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser recall
FDA recall D-0356-2024 · initiated Feb 19, 2024
Seatex LLC recalled PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser in Feb 2024 — an FDA Class II recall (D-0356-2024) because CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
The manufacturing process itself
The FDA found the process itself out of compliance, usually before any defective product was identified.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 1,450 cases
Details
- Product
- PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G cases, mountain spring scent, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471.
- Recalling company
- Seatex LLC
- Classification
- Class II
- Status
- Terminated
- Type
- Voluntary: Firm initiated
- Distribution
- Nationwide in the US and Puerto Rico
- Initiated
- Feb 19, 2024
- FDA report date
- Mar 6, 2024
Frequently asked
- Was PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser recalled?
- Seatex LLC recalled PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser in Feb 2024 — an FDA Class II recall (D-0356-2024) because CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser recalled?
- Per the FDA enforcement record, the reason for recall D-0356-2024 was: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
- Is a recalled PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser are affected?
- Distributed: Nationwide in the US and Puerto Rico. The recall covers these lots — Lot #s: a) 263647, Exp. 06/09/2024; 271382, Exp. 01/18/2025; b) 261675, Exp. 04/09/2024; 263647, Exp. 06/09/2024; 272766, Exp.02/15/2025.. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0356-2024.