Superior Glove Works recalls Synergy Hand Sanitizer due to acetaldehyde impurities exceeding safety limits. This may pose health risks if used improperly. Learn what to do.
CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.
Superior Glove Works is recalling Synergy Hand Sanitizer products because FDA testing found harmful acetaldehyde impurities. Using these products could potentially lead to health issues if the impurities cause disease.
The hand sanitizer contains acetaldehyde impurities above the safety limits set by the FDA. This impurity could potentially cause health issues, especially in people with sensitive health conditions or those using the product frequently.
People who own or use Synergy Hand Sanitizer products made by Superior Glove Works in Canada. Those most at risk are individuals with sensitive health conditions or those using the product frequently.
Check for Synergy Hand Sanitizer, Non-Sterile Solution bottles labeled 'Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL' with UPC 779406201594. Products made in Canada with lot number 200513TA and expiration date 05/2023 are affected.
Look for the UPC code 779406201594 and lot number 200513TA on the bottle.
The FDA found acetaldehyde impurities above safety limits, so it may pose health risks. Use only if you have no sensitive health conditions.
Check for the UPC 779406201594 and lot number 200513TA on the bottle. Products made in Canada with expiration date 05/2023 are affected.
The recall does not specify a remedy, so contact Superior Glove Works for guidance.
We’ve drafted a message you can send Superior Glove Works to request your refund or repair — edit it as you like.
Subject: Recall D-1537-2022 — Superior Glove Works Superior Glove Works Hello, I own a Superior Glove Works that is covered by recall D-1537-2022 from Superior Glove Works. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
