CLASS I Drug recall · Reported 6 Jan 2021 · FDA Enforcement Report
Happy Ducts Compress, www.wishgardenherbs.com, Boulder, CO. recalled
Wishgarden Herbs, Incorporated is recalling Happy Ducts Compress, www.wishgardenherbs.com, Boulder, CO. 80301, distributed nationwide in the US. The recall was initiated on 25 Sep 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-0218-2021
- FDA event ID
- 86709
- Recalling firm
- Wishgarden Herbs, Incorporated, Louisville, CO
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 25 Sep 2020
- FDA classified
- 7 Jan 2021
- Reported
- 6 Jan 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Cronobacter
Timeline
| 25 Sep 2020 | Recall initiated by company | |
| 6 Jan 2021 | Published in enforcement report | +103 days |
| 7 Jan 2021 | Classified by FDA | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of a Non-Sterile Product: Product tested positive for Cronobacter Sakazakii.
Product as listed by the FDA
Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5
Where it was distributed
Distributed Nationwide in the USA, Egypt and Canada.
Questions about this recall
Is Happy Ducts Compress, www.wishgardenherbs.com, Boulder, CO. 80301 recalled?
Yes. Wishgarden Herbs, Incorporated recalled Happy Ducts Compress, www.wishgardenherbs.com, Boulder, CO. 80301 on 25 Sep 2020. The recall is Class I and its status is Terminated. Recall number D-0218-2021.
Why was it recalled?
Microbial Contamination of a Non-Sterile Product: Product tested positive for Cronobacter Sakazakii.
Which lots are affected?
Lot # 53664, Exp 08/2022
Where was it sold?
Distributed Nationwide in the USA, Egypt and Canada.
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.
More recalls from Wishgarden Herbs, Incorporated
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Cord Care Powder, Wishgarden Herbs, Inc., Boulder, CO recalled | Wishgarden Herbs, Incorporated | Cronobacter | Nationwide |
| Drug | CLASS I | Goldenseal Powder, WishGarden Herbs, Inc., Boulder, CO recalled | Wishgarden Herbs, Incorporated | Cronobacter | Nationwide |