Alcohol Sanitizer Spray Recalled Due to Microbial Contamination

Key Takeaways:

• The US Food and Drug Administration (FDA) has issued a voluntary Class II recall for alcohol sanitizer spray. The affected batch has been identified as Lot E2612116 (expires April 2029), affecting 5 drums.
• The recall was initiated by Zep Inc due to microbial contamination, a quality issue that may cause temporary or medically reversible adverse health consequences.
• Alcohol sanitizer spray is used to disinfect hands and remove bacteria and other microorganisms. It can also be used as a first-aid antiseptic.

The FDA has issued a Class II recall for alcohol sanitizer spray, affecting 5 drums. This product is manufactured by Zep Inc based in Emerson, Georgia. The recall was initiated by Zep Inc on May 22, 2026, and received a Class II classification on June 10, 2026. A Class II classification means the use of this product may cause temporary or medically reversible adverse health consequences or has a low chance of causing serious adverse health consequences.

The recall was initiated due to microbial contamination of sterile products. This deficiency affects Lot E2612116, which will expire in April 2029. Zep Inc sent out a public notice via letter; no public press release has been issued for this recall.

Alcohol sanitizer spray is used to reduce or eliminate bacteria and other microorganisms found on bare hands. It can supplement regular hand washing in industries such as food processing, food service, health care, emergency services, and police departments. It can also be used as a first-aid antiseptic to protect against skin infection from minor cuts, scrapes, or burns. Pharmacists should identify and quarantine Lot E2612116, remove it from inventory, and coordinate with prescribers to provide an alternative supply.

Reference

FDA. Enforcement Report. June 17, 2026. Accessed June 17, 2026. https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=220850