Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm
FDA Recall Z-0856-2022 · Posted None
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Recalling FirmSA3, LLC
Recall StatusTerminated
Product CodeOLR
Date Initiated2022-02-21
Date Terminated2024-05-15
Product Quantity156 units
Reason for Recall
Due to failure of microbial testing for total aerobic microbial count (TAMC).
Firm Action
On 02/21/2022, the firm emailed an Urgent Recall Notification to customers informing them that the recall has been initiated due to the affected lot's microbial testing results for total aerobic microbial count (TAMC exceeded specifications prior to expiry of the gel.
Customer are instructed to:
1. Immediately examine your inventory and quarantine product subject to this recall.
2. Immediately discontinue use and distribution of the identified lot number.
3. To request a prepaid shipping label, complete and return the enclosed Customer Market
Withdrawal Return Response Form via email at [email protected] or via fax at 888-502-1669.
4. If customer have further distributed this product to other wholesalers or pharmacies, please identify and notify them at once of this product market recall. The Recall notification and return response form should be include when notifying these customers.
5. Return the affected product to:
Alexso, Inc.
c/o Recall
2317 Cotner Ave
Los Angeles, CA 90064
For any questions, contact the Recalling Firm at (888)-495-6078, Monday through Friday 9:00 AM to 5:00 PM PST or email at [email protected].
On 03/07/2022, the firm emailed an updated "URGENT: Medical Device Market Removal" letter which informs customers of the potential risks/harms/hazards associated with use of the affected products and added that it is recommended that physicians monitor their patents for potential adverse reactions and events as a result of use of the affected product.
Root Cause
Under Investigation by firm
Distribution Pattern
U.S. Nationwide distribution in the states of CA, FL and GA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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