Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially cause disease, For use when soap and water are not available, Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL bottles, Made and Distributed by: Superior Glove Works Ltd., 36 Vimy Street, Acton, Ontario, L7J 1S1, Canada, Made in Canada, UPC: 779406201594.

CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.

Recall #: D-1537-2022
Affected scope: 7,296 bottles
Initiated: September 1, 2022

Compiled from official public sources by the publisher. · Updated September 2026

Verify with FDA Drug →

View my saved recalls

Superior Glove Works, LTD. recalled Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially… - a moderate-severity action.

Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially… was recalled by Superior Glove Works, LTD. in September 21, 2022. Reason: CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, a…. Check the official notice for the remedy. Verify recall #D-1537-2022 with the FDA Drug before acting.

The recall

Superior Glove Works, LTD. issued this moderate-severity FDA Drug recall-CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, a….

Moderate
severity level: Class II
classification: September 21, 2022
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-1537-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 3 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially cause disease, For use when soap and water are not available, Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL bottles, Made and Distributed by: Superior Glove Works Ltd., 36 Vimy Street, Acton, Ontario, L7J 1S1, Canada, Made in Canada, UPC: 779406201594.

Reason for recall

CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	D-1537-2022
Date reported	September 21, 2022
Date initiated	September 1, 2022
Recalling firm	Superior Glove Works, LTD.
Firm location	Acton
Affected scope	7,296 bottles
Distribution	Nationwide in the US.

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (D-1537-2022) and product description against the item you own. Search the archive
Confirm the current status with FDA Drug before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on September 21, 2022. Severity: Moderate. Recall number: D-1537-2022.

Where was the recalled product distributed? ▼

Distribution: Nationwide in the US..

Should I stop using a recalled medication or medical device? ▼

Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

Magnesium Citrate SALINE LAXATIVE, Oral S… 2022-09-21 Magnesium Citrate SALINE LAXATIVE, Oral S… 2022-09-21 Magnesium Citrate SALINE LAXATIVE, Oral S… 2022-09-21 Bupivacaine HCl 0.375% w/v and Lidocaine … 2022-09-21

Similar Cosmetics & Personal Care · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Triamcinolone Acetonide cream, 0.1%, 80 g… 2022-09-21 BE Jewel Accessories Recalls Children's H… 2022-09-29 Colgate Anticavity Fluoride Toothpaste, O… 2022-09-07 Colgate Anticavity Fluoride Toothpaste, O… 2022-09-07

Compare this recall with Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 7… → · All Cosmetics & Personal Care recalls

This recall: FDA Drug, reported September 21, 2022. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026