H & H Remedies, LLC recalls Vapor Ointment packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; and d) 8 oz jars. Mfg & Sold by: H & H Remedies, LLC c/o
H & H Remedies recalls vapor ointment in 1/8 oz, 2 oz, 4 oz, and 8 oz jars due to CGMP deviations. Affected products were manufactured from Lot H20-01V to H20-10V.
Lower-risk recall
CGMP Deviations
Contact the company & request your remedy
What happened, in plain English
H & H Remedies is recalling vapor ointment in 1/8 ounce, 2 ounce, 4 ounce, and 8 ounce jars because of manufacturing quality control issues. This recall does not pose a risk of injury but requires consumers to stop using the product to avoid potential quality problems. Read more at govinfonow.com/recall/36705-h-h-remedies-vapor-ointment-recall-cgmp-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/36705-h-h-remedies-vapor-ointment-recall-cgmp-deviations · Updated October 4, 2026 · FDA enforcement record: FDA #D-0073-2021
Cite this page
“H & H Remedies Vapor Ointment Recall: CGMP Deviations.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36705-h-h-remedies-vapor-ointment-recall-cgmp-deviations. Based on FDA recall #D-0073-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0073-2021%22&limit=1).
Why it’s dangerous
The product was made under CGMP (Current Good Manufacturing Practices) deviations, meaning the manufacturing process did not meet quality standards. This could result in the ointment not being as effective as intended for skin care.
Who’s affected
Owners of vapor ointment jars manufactured from Lot H20-01V to H20-10V are affected. People using these products for skin care are most at risk of receiving substandard medication.
How to tell if you have this one
Check for vapor ointment jars labeled with Lot numbers H20-01V through H20-10V. The product comes in 1/8 ounce, 2 ounce, 4 ounce, and 8 ounce sizes.
- Brand
H & H Remedies- Category
Drug
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 II- Status
Terminated- Distribution
Nationwide in the United States
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0071-2021 | Union (black) salve packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; d) 8 oz.; e) 16 oz.; and f) 32 oz. jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663; Lot #: H20-01S thru H20-12S | 939 jars |
| D-0072-2021 | White Liniment packaged in a) 1 oz; b) 4 oz.; and c) 6 oz bottles. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663; Lot #: H20-01W thru H20-84W | 365 bottles |
| D-0073-2021 | Vapor Ointment packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; and d) 8 oz jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663; Lot #: H20-01V thru H20-10V | 252 jars |
What to do — step by step
Check Product Lot Number
Look for the lot number on the jar, which should be between H20-01V and H20-10V.
Stop Using Product
If the lot number matches the affected range, stop using the product immediately.
Questions people ask
What is the recall for?
H & H Remedies is recalling vapor ointment in 1/8 oz, 2 oz, 4 oz, and 8 oz jars due to CGMP deviations in manufacturing.
How can I tell if I have the recalled product?
Check the lot number on the jar, which should be between H20-01V and H20-10V. The product comes in 1/8 ounce, 2 ounce, 4 ounce, and 8 ounce sizes.
Do I need to return the product?
The recall record does not specify a return process, so no action is required beyond stopping use if the product is affected.
Contact H & H Remedies
We’ve drafted a message you can send H & H Remedies to request your refund or repair — edit it as you like.
Subject: Recall D-0073-2021 — H & H Remedies H & H Remedies Hello, I own a H & H Remedies that is covered by recall D-0073-2021 from H & H Remedies. 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-0073-2021 (October 21, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0073-2021 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.