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Stop using now Drug recall · FDA · Published September 25, 2020

Wishgarden Herbs Happy Ducts Compress Recall: Microbial Contamination Risk

Wishgarden Herbs recalls Happy Ducts Compress 3 oz. plastic jars due to Cronobacter Sakazakii contamination. Affected lots may cause illness; consumers should stop using and contact the company.

🇺🇸 FDA recall #D-0218-2021DrugWishgarden Herbs ›
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Contact the company

Official pagewww.wishgardenherbs.com
Recalling firmWishgarden Herbs, Incorporated321 S Taylor Ave Unit 100 · Louisville, CO 80027-3600
✎ GovInfoNow plain-language explainer

Wishgarden Herbs is recalling Happy Ducts Compress 3 oz. plastic jars because they tested positive for Cronobacter Sakazakii, a bacteria that can cause serious illness. This recall affects products with lot number 53664 that expired August 2022. Consumers should stop using these products immediately to avoid potential health risks. Read more at govinfonow.com/recall/36760-wishgarden-herbs-happy-ducts-compress-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/36760-wishgarden-herbs-happy-ducts-compress-recall-microbial-contamination-risk · Updated October 4, 2026 · FDA enforcement record: FDA #D-0218-2021

Cite this page

“Wishgarden Herbs Happy Ducts Compress Recall: Microbial Contamination Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36760-wishgarden-herbs-happy-ducts-compress-recall-microbial-contamination-risk. Based on FDA recall #D-0218-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0218-2021%22&limit=1).

The FDA announced on September 25, 2020, that Wishgarden Herbs, Incorporated voluntarily recalled Happy Ducts Compress due to microbial contamination. The product tested positive for Cronobacter Sakazakii.

How to tell if you have it

  • Brand: Wishgarden Herbs
  • Product: Happy Ducts Compress, 3 oz. plastic jar
  • UPC: 6 56490 20223 5
  • Lot #: 53664
  • Expiration: 08/2022
  • Sold at: www.wishgardenherbs.com, Boulder, CO. 80301

The hazard

The FDA stated the non-sterile product tested positive for Cronobacter Sakazakii. The recall is classified as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include Broadway Joe's Pain Cream Recall (2026-08-21), Blaine Labs Revitaderm Wound Gel Recall (2026-04-08) and Beekeeper's Naturals Saline Nasal Spray Recall (2026-06-01).

How to tell if you have this one

Check for the product name 'Happy Ducts Compress', 3 oz. plastic jar, and lot number 53664 (expired August 2022). The product was sold online at www.wishgardenherbs.com from Boulder, CO.

  • Brand
    Wishgarden Herbs
  • Product
    Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5
  • Category
    Drug
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    Distributed Nationwide in the USA, Egypt and Canada.
Recall numberProduct, codes & lotsQuantity
D-0218-2021Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5; Lot # 53664, Exp 08/202246 jars
D-0219-2021Cord Care POWDER, 0.25 oz. (7 g) plastic jars, Wishgarden Herbs, Inc., Boulder, CO 80301. UPC 6-56490 24730 4; Lot #: P227 - Exp. 11/2020; P228 - Exp. 12/2020; P229 - Exp. 02/2021; P230 - Exp. 04/2021; P231 - Exp. 06/2021; P232 - Exp. 09/2021; P233 - Exp. 01/2022; P234 - Exp. 05/2022; P235 - Exp. 08/20221651 jars
D-0220-2021Goldenseal POWDER, 0.25 oz. (7 g) plastic jars, WishGarden Herbs, Inc., Boulder, CO 80301. UPC 6 56490 64137 9; P116 - Exp. 12/2020; P117 - Exp. 05/2021; P118 - Exp. 10/2021; P119 - Exp. 01/2022; P120 - Exp. 04/2022298 jars
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using Happy Ducts Compress 3 oz. plastic jars with lot number 53664 that expired August 2022.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Distributed Nationwide in the USA, Egypt and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 3.7 years after the firm started it.

1. Firm started the recall: Sep 25, 202012. Published in FDA’s Enforcement Report: Jan 6, 202123. FDA classified it Class I: Jan 7, 202134. FDA terminated the recall: May 29, 2024420202024
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Take action

Contact Wishgarden Herbs

We’ve drafted a message you can send Wishgarden Herbs to request your refund or repair — edit it as you like.

Subject: Recall D-0218-2021 — Wishgarden Herbs Happy Ducts Compress Recall: Microbial Contamination Risk

Hello,

I own a Wishgarden Herbs Happy Ducts Compress Recall: Microbial Contamination Risk that is covered by recall D-0218-2021 from Wishgarden Herbs.

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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Where this comes from

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.

  • Official source: FDA Recall #D-0218-2021 (September 25, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0218-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA