FDA-Drug2026-10-27Class IIPROCESSING DEFECT

Lynx antiseptic handsoap recalled for manufacturing deviations

OTHERNationwide distributionDrugs

What this means

ABC Compounding Co. is recalling about 9,252 bottles of Lynx LX0864 peachy-foam antiseptic handsoap, 1000 mL (33.8 fl oz), which were distributed nationwide. The FDA classified the recall as Class II because the manufacturer did not fully meet current good manufacturing practice (CGMP) quality standards. No injuries have been reported.

  • Check the bottle for UPC 711808210804 and product code LX0864.
  • If your bottle matches, contact ABC Compounding Co. or the place you bought it for guidance on returns or refunds.
  • Ask your pharmacist or the seller whether you should keep using the product until you hear back.
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The agency's original wording
Hazard

CGMP Deviations

Intended for
All ages
Illnesses reported
None reported
Sold states
US Nationwide
Affected count
9252 bottles
Manufactured in
2600 Dogwood Dr Se, Conyers, Georgia, United States
Products
Lynx, LX0864 peachy-foam antiseptic handsoap, 1000 ML (33.8 FL OZ.) Manufactured by: ABC Compounding Co., INC., 2500 Dogwood Dr., Conyers, GA 30013, UPC 711808210804.

UPC codes

  • 711808210804

Products in this recall · 19

The agency lists each product in this recall separately. Check every one you might have.

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0092-2027

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