KVK Tech recalls 100-count 30mg Phentermine Hydrochloride Capsules (NDC 10702-028-01) made in USA with lot numbers 18350A/18351A. The recall is for cGMP deviations, meaning possible quality issues in production.
cGMP deviations
KVK Tech is recalling 100-count bottles of 30mg Phentermine Hydrochloride Capsules due to manufacturing quality issues. This recall affects prescription-only products made in the USA with specific lot numbers. The issue could lead to potential product quality concerns, though the exact risk is not specified in the recall.
The recall mentions cGMP deviations, which are regulatory standards for manufacturing quality. This indicates possible issues in the production process that could affect product safety or effectiveness. However, the specific nature of the deviations and their potential impact are not detailed in the recall.
Prescription holders of the 30mg Phentermine Hydrochloride Capsules with lot numbers 18350A or 18351A. Individuals using these capsules for weight management are most at risk due to the manufacturing deviations.
Check your prescription bottle for the brand KVK Tech, product name Phentermine Hydrochloride Capsules, 30mg, 100-count, and lot numbers 18350A or 18351A. The product was made in the USA with expiration date 6/30/2027.
Verify your bottle has lot numbers 18350A or 18351A and expiration date 6/30/2027.
The recall is for cGMP deviations, which are manufacturing quality issues that could affect product safety or effectiveness.
The recall does not specify a remedy, so you should check the product details to confirm if it's affected and contact your healthcare provider for advice.
The recall does not describe specific hazards that could cause injury, so the risk level is unknown.
We’ve drafted a message you can send KVK Tech to request your refund or repair — edit it as you like.
Subject: Recall D-0446-2025 — KVK Tech KVK Tech Hello, I own a KVK Tech that is covered by recall D-0446-2025 from KVK Tech. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
