Solco Recalls Gabapentin 800mg Due to Label Mix-Up
Solco Healthcare recalls specific lots of Gabapentin 800mg tablets because bottles labeled as 800 mg may actually contain 600 mg.
Use caution until it’s fixed
Labeling: Label Mix-Up.some bottles labeled as Gabapentin 800 mg contain Gabapentin 600 mg
Contact the company
What happened, in plain English
Solco Healthcare US LLC is recalling a specific lot of Gabapentin Tablets, USP, 800 mg, distributed in Mason, OH. The issue involves a labeling error where some bottles marked as containing 800 mg tablets actually contain 600 mg tablets. This discrepancy could lead to patients receiving an incorrect dosage. Read more at govinfonow.com/recall/41031-solco-recalls-gabapentin-800mg-due-to-label-mix-up.
Source Summary by GovInfoNow · govinfonow.com/recall/41031-solco-recalls-gabapentin-800mg-due-to-label-mix-up · Updated October 11, 2026 · FDA enforcement record: FDA #D-0155-2018
Cite this page
“Solco Recalls Gabapentin 800mg Due to Label Mix-Up.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/41031-solco-recalls-gabapentin-800mg-due-to-label-mix-up. Based on FDA recall #D-0155-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0155-2018%22&limit=1).
Why it’s dangerous
The hazard is a labeling mix-up where bottles labeled as Gabapentin 800 mg contain Gabapentin 600 mg. Taking the wrong dose can result in under-treatment if more pills are taken to compensate, or over-medication if the patient assumes the label is correct but the content is different.
Who’s affected
Patients in Mason, OH, who purchased or were prescribed the recalled Gabapentin Tablets from this specific distribution lot are affected. Individuals relying on the precise 800 mg dosage for their treatment are at risk of receiving an incorrect strength.
How to tell if you have this one
Check for Gabapentin Tablets, USP, 800 mg, 500-count, Rx only. Look for NDC 43547-0333-50 and Lot # 7700656A. The product was distributed by Solco Healthcare US LLC in Mason, OH.
- Brand
Solco Healthcare- Category
Drug
What to do — step by step
Check your medication
Verify if your Gabapentin bottles match NDC 43547-0333-50 and Lot # 7700656A.
Contact your pharmacist
If you have the recalled product, speak with your pharmacist or healthcare provider immediately to determine the next steps for replacement or disposal.
Where it went and when
Where it was distributed
Distributed in Ohio.
FDA distribution: “Product was distributed in Mason, OH.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Ohio.
Recall timeline
FDA terminated this recall 15 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-0155-2018 (December 4, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0155-2018 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.