thiamine HCl
Lack of Assurance of Sterility
Yes — there is an active recall. 12 ongoing FDA recalls mention Thiamine (39 total). Check the affected lots below.
Most common reason: Sterility / contamination (31 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Thiamine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Lack of Assurance of Sterility
cGMP violations
Presence of Particulate Matter.
Presence of Particulate Matter.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Presence of Particulate Matter: Presence of foreign substances were reported in vials at the pharmacy.
Lack of Assurance of Sterility
Lack of assurance of sterility.
Lack of assurance of sterility.
Lack of assurance of sterility.
Labeling: Incorrect or Missing Lot and/or Exp Date: Cartons with the correct lot number 200906 contain vials labeled with the incorrect lot number 200901.
Lack of Assurance of Sterility
Lack of Sterility Assurance.
Lack of sterility assurance.
Lack of sterility assurance.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
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