FDA recall, , Moderate risk
Tychasis Coats Aloe Lotion, Creme and Liniment
Tychasis Coats Aloe Lotion, Creme and Liniment have failed stability specifications.
Summary by Recall Canary from the FDA notice
What happened
BioMed Laboratories, LLC of Dallas, Texas voluntarily recalled Tychasis Coats Aloe Lotion, Tychasis Coats Aloe Liniment, and Tychasis Coats Aloe Creme because the products failed stability specifications, including viscosity and appearance results that did not align with established specifications. The recall began October 15, 2026, and was added to the FDA's Enforcement Report on November 2, 2026.
The products were manufactured for Tychasis Corporation of Dallas, TX 75227, and distributed in Texas only. The lotion and liniment came in 0.5 oz sample bottles, 8 oz bottles, and 33 oz bottles; the creme came in 4 oz and 16 oz jars. Customers were notified by letter.
3 photos
What to do
The FDA notice gives no instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
3 products
Affected if its lot code and NDC are listed under that product.
An NDC (National Drug Code) is usually printed on the drug's label.
Tychasis Coats Aloe Lotion (Allantoin 0.5%)
- NDC
- 70211-704-08
- 70211-704-33
- Lot code
- 011636
- 0001882604
- 0001987649
- 008943
- 0001893936
Tychasis Coats Aloe Liniment (Methyl salicylate 10%)
- NDC
- 70211-704-08
- 70211-704-33
- Lot code
- 0.5
- 0001882607
- 0001882605
- 0001916439
- 0001882606
Tychasis Coats Aloe Creme (Allantoin 0.5%)
- NDC
- 70211-703-04
- 70211-703-16
- Lot code
- 0002011787
- 0001932354
- 0002049590
Recall details
- Posted by FDA
- Recall began
- Status
- Open
- Weekly archive
- Listed the week of Nov 2, 2026
- Sold in
- Recalled by
- BioMed Laboratories, LLC.Dallas, Texas
- Hazard
- Quality testing problem
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- FDA event number
- 100153
- Recall numbers
- D-0159-2027 to D-0161-2027
- Recall type
- Voluntary: Firm initiated
- How the company first told customers
- Letter
All recalls from BioMed Laboratories, LLC.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA posts a recall by adding it there.
BioMed Laboratories began the recall
FDA posted the recall to its Enforcement Report and rated it Class II (moderate risk)
Added to Recall Canary
