CLASS I Drug recall · Reported 29 Jul 2020 · FDA Enforcement Report
Mystic Shield Protection, Alcohol Antiseptic recalled
Transliquid Technologies is recalling Mystic Shield Protection, Alcohol Antiseptic 70%, Topical Solution, Antiseptic Hand Rub, distributed nationwide in the US. The recall was initiated on 29 Jun 2020 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1408-2020
- FDA event ID
- 85957
- Recalling firm
- Transliquid Technologies, Spring, TX
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 29 Jun 2020
- FDA classified
- 24 Jul 2020
- Reported
- 29 Jul 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
- Drug class
- Creams, Ointments & Gels
Timeline
| 29 Jun 2020 | Recall initiated by company | |
| 24 Jul 2020 | Classified by FDA | +25 days |
| 29 Jul 2020 | Published in enforcement report | +5 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Chemical Contamination: Presence of Undeclared Methanol
Product as listed by the FDA
Mystic Shield PROTECTION, ALCOHOL ANTISEPTIC 70%, Topical Solution, Antiseptic Hand Rub, Non-sterile Solution, Extra strength Formula*, 8.45 fl. oz. (250 ml) bottle, Labeled with green or blue labels, Manufactured by Mystic Intl S.A. de C.V. UPC barcode: 7 87790 33952 6
Where it was distributed
Distributed Nationwide in the US
Questions about this recall
Is Mystic Shield Protection, Alcohol Antiseptic 70%, Topical Solution, Antiseptic Hand Rub recalled?
Yes. Transliquid Technologies recalled Mystic Shield Protection, Alcohol Antiseptic 70%, Topical Solution, Antiseptic Hand Rub on 29 Jun 2020. The recall is Class I and its status is Terminated. Recall number D-1408-2020.
Why was it recalled?
Chemical Contamination: Presence of Undeclared Methanol
Which lots are affected?
Lots: All Lots
Where was it sold?
Distributed Nationwide in the US
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.