CLASS II Drug recall · Reported 5 Jun 2019 · FDA Enforcement Report
Inoderm Antiseptic Hand Soap (E-2), .6% recalled by Inopak
Inopak is recalling Inoderm Antiseptic Hand Soap (E-2), .6% (incorrectly labeled on bags as 75%) Pcmx/pouches, distributed nationwide in the US. The recall was initiated on 22 Apr 2019 and the FDA has classified it as Class II.
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-1313-2019
- FDA event ID
- 82645
- Recalling firm
- Inopak, Ringwood, NJ
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 22 Apr 2019
- FDA classified
- 29 May 2019
- Reported
- 5 Jun 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
Timeline
| 22 Apr 2019 | Recall initiated by company | |
| 29 May 2019 | Classified by FDA | +37 days |
| 5 Jun 2019 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Product as listed by the FDA
INODERM Antiseptic Hand Soap (E-2), .6% (incorrectly labeled on bags as 75%) PCMX, 800ml/27fl.oz.pouches (NDC 058575-110), 12 x 800 Bag-N-Box pouches per case (NDC 058575-110-80), 5014-404-NB; INOPAK, 24 Executive PKWY, Ringwood, NJ 07456.
Where it was distributed
Nationwide in the USA
Questions about this recall
Is Inoderm Antiseptic Hand Soap (E-2), .6% (incorrectly labeled on bags as 75%) Pcmx/pouches recalled?
Yes. Inopak recalled Inoderm Antiseptic Hand Soap (E-2), .6% (incorrectly labeled on bags as 75%) Pcmx/pouches on 22 Apr 2019. The recall is Class II and its status is Terminated. Recall number D-1313-2019.
Why was it recalled?
CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.
Which lots are affected?
Batch #: 7074
Where was it sold?
Nationwide in the USA
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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.
More recalls from Inopak
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|---|---|---|---|---|---|
| Drug | CLASS II | Aquacil instant foaming hand sanitizer recalled by Inopak | Inopak | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Antibacterial Foaming Hand Wash With Moisturizers labeled recalled | Inopak | Foreign Material | Nationwide |
| Drug | CLASS II | Sani-Guard-SF Waterless Foam Hand Sanitizer, Ethyl Alcohol recalled | Inopak | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Instant Waterless Hand Sanitizer, Ethyl Alcohol recalled by Inopak | Inopak | Foreign Material | Nationwide |
| Drug | CLASS II | Antibacterial Hand Soap, Healthcare recalled by Inopak | Inopak | Manufacturing (CGMP) Deviations | Nationwide |