KVK-Tech, Inc. recalls Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK
KVK Tech recalls 500mL methylphenidate oral solution due to fiber particles. This may cause injury if ingested. Consumers should contact the manufacturer for details.
Lower-risk recall
Presence of Foreign Substance; Fiber particles.
Contact the company & request your remedy
What happened, in plain English
KVK Tech is recalling a 500mL bottle of methylphenidate oral solution because it contains foreign fiber particles. This could cause injury if the particles are ingested. The recall is for prescription-only medication. Read more at govinfonow.com/recall/37870-kvk-tech-methylphenidate-solution-recall-foreign-fiber-particles-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/37870-kvk-tech-methylphenidate-solution-recall-foreign-fiber-particles-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #D-0142-2020
Cite this page
“KVK Tech Methylphenidate Solution Recall: Foreign Fiber Particles Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37870-kvk-tech-methylphenidate-solution-recall-foreign-fiber-particles-hazard. Based on FDA recall #D-0142-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0142-2020%22&limit=1).
Why it’s dangerous
The product contains fiber particles that could be ingested and cause injury. This is a foreign substance hazard in a medication product.
Who’s affected
Prescription patients using the specific 50:00mL bottle of methylphenidate oral solution. Those with the batch number 15315A are most at risk.
How to tell if you have this one
Check for the 500mL bottle labeled 'Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, Sugar Free Alcohol Free'. The batch number 15315A and expiration date 02/2021 are key identifiers.
- Brand
KVK Tech- Category
Drug
What to do — step by step
Check Product Details
Look for the batch number 15315A and expiration date 02/2021 on the bottle.
Questions people ask
Is this product safe to use?
The product contains foreign fiber particles that could cause injury if ingested, so it is not safe to use.
How can I tell if I have the recalled product?
Check for the 500mL bottle with batch number 15315A and expiration date 02/2021.
What should I do if I have this product?
The recall does not specify a remedy, so contact KVK Tech for further instructions.
Contact KVK Tech
We’ve drafted a message you can send KVK Tech to request your refund or repair — edit it as you like.
Subject: Recall D-0142-2020 — KVK Tech KVK Tech Hello, I own a KVK Tech that is covered by recall D-0142-2020 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.
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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-0142-2020 (October 4, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0142-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.