PeriGiene
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Yes — there is an active recall. 12 ongoing FDA recalls mention Chloroxylenol (16 total). Check the affected lots below.
Most common reason: cGMP deviation (6 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Chloroxylenol. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
cGMP Deviations: Out of specification results for micro in hand soap products.
cGMP Deviations: Out of specification results for micro in hand soap products.
cGMP Deviations: Out of specification results for micro in hand soap products.
cGMP Deviations: Out of specification results for micro in hand soap products.
cGMP Deviations: Out of specification results for micro in hand soap products.
CGMP Deviations: initiated due to violations of CGMP manufacturing practices
CGMP Deviations
CGMP Deviations
Labeling: Label mix-up - the label on the product may not match the formula in the bottle.
Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or has illegible lot and expiry codes, as well as defective or cracked caps.
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