The Shaman Botanicals Alkaloids recall 2026 involves White Vein chewable tablets that may contain higher-than-declared levels of 7-Hydroxymitragynine, prompting a voluntary nationwide recall.
Here’s what consumers need to know.
What Is the Shaman Botanicals Alkaloids Recall About?
Shaman Botanicals, LLC has announced a voluntary nationwide recall of:
Alkaloids Chewable Tablets – White Vein
The Shaman Botanicals Alkaloids recall was announced after internal testing revealed potency inconsistencies.
The recall was initiated after testing found that the product contains 7-Hydroxymitragynine (7-OH) at levels exceeding the labeled amount of 7.5 mg per tablet.
This means consumers may unknowingly ingest a stronger dose than intended.
Affected Products
The recall includes:
- 2-Count Bag – UPC: 810057763724
- 20-Count Bag – UPC: 810057763830
- 30-Count Bottle – UPC: 810057763779
- Lot Number: B# AAW.501.3
- All expiration dates under this lot
The product was distributed nationwide, including:
- Online sales
- Wholesale distribution
- Retail outlets
Why Is This Recall Serious?
The concern is not contamination — it is potency.
The product contains higher-than-declared levels of 7-Hydroxymitragynine (7-OH), a compound known for producing opioid-like effects.
Higher potency may increase the risk of:
- Sedation
- Respiratory depression
- Dizziness
- Nausea
- Increased dependence risk
- Other adverse effects
Even when labeled amounts appear small, potency inconsistencies in supplements can create unpredictable health risks.
The Shaman Botanicals Alkaloids recall is a reminder that supplement potency errors can pose serious health risks.
As of the recall announcement, no adverse events had been reported.
What Is 7-Hydroxymitragynine?
7-Hydroxymitragynine (7-OH) is an alkaloid derived from kratom (Mitragyna speciosa). It is known to interact with opioid receptors in the body.
The FDA has previously warned about the risks associated with products containing concentrated 7-OH, especially when not properly regulated or labeled.
Supplements containing undeclared or excessive active ingredients present particular risks because consumers may not realize they are consuming stronger doses.
What Consumers Should Do Immediately
If you have purchased Alkaloids Chewable Tablets – White Vein, take the following steps:
1️⃣ Stop Using the Product
Do not consume additional tablets.
2️⃣ Check the Lot Number
Look for Lot B# AAW.501.3 on the packaging.
3️⃣ Return for Refund
Consumers may return affected products for a refund through the company’s recall portal:
https://recall.cbdamericanshaman.com
4️⃣ Monitor for Symptoms
If you experience unusual symptoms such as:
- Extreme drowsiness
- Breathing difficulties
- Confusion
- Unusual heart rate
Contact a healthcare provider immediately.
5️⃣ Report Adverse Reactions
Adverse events can be reported to the FDA MedWatch program.
Company Contact Information
Consumers with questions may contact the company’s Quality Department:
- Phone: 855-427-7386
- Email: Quality@CBDAmericanShaman.com
- Hours: Monday – Friday, 9 AM – 5 PM CST
How to Identify the Product
The recalled product is sold as chewable tablets in:
- Small bags (2-count or 20-count)
- Bottled packaging (30-count)
Check the UPC codes and lot number listed above before use.
If you are unsure, do not consume it.
Why Supplement Recalls Matter
Dietary supplements are not regulated as strictly as prescription medications. When manufacturing or labeling errors occur, consumers may unknowingly expose themselves to:
- Incorrect dosages
- Undeclared ingredients
- Potency inconsistencies
That’s why recall alerts like this are critical.
Even when no injuries are reported, correcting labeling or formulation issues helps prevent future harm.
If You Already Consumed the Product
If you have taken this supplement and feel fine, there is no need to panic.
However, you should:
- Stop using it
- Monitor your health
- Contact a provider if symptoms appear
If you are taking other medications or have underlying conditions, consult your healthcare provider for guidance.
Official Recall Announcement
The recall was announced by the U.S. Food and Drug Administration and published on the FDA recall portal.
You can view the official FDA announcement here: fda.gov
Final Thoughts
When it comes to supplements, accurate labeling matters.
This recall serves as a reminder that even small dosage discrepancies can create unintended risks.
If you have this product, stop using it and request a refund.
Stay informed. Stay safe.
For more current safety alerts, visit our updated Product Recall Center here: https://everydayanswers.online/cs-beef-packers-ground-beef-recall-feb-2026/