Golden State Medical Supply Inc. recalls TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg, Rx Only a)100-count bottles (NDC 60429-588-01) b) 500-count bottle (NDC
Golden State Medical Supply recalls 50mg Tramadol tablets with incorrect package inserts that may lead to improper dosing. Affected lots have specific NDC numbers and expiration dates.
Lower-risk recall
Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored 50 mg tablet.
Contact the company & request your remedy
What happened, in plain English
Golden State Medical Supply is recalling 50mg Tramadol hydrochloride tablets because the patient leaflets contain incorrect dosing instructions for unscored tablets. This could lead to improper dosing if someone tries to split the tablet without scoring it. Read more at govinfonow.com/recall/37375-golden-state-medical-supply-recalls-50mg-tramadol-tablets-due-to.
Source Summary by GovInfoNow · govinfonow.com/recall/37375-golden-state-medical-supply-recalls-50mg-tramadol-tablets-due-to · Updated October 5, 2026 · FDA enforcement record: FDA #D-0856-2020
Cite this page
“Golden State Medical Supply recalls 50mg Tramadol tablets due to incorrect dosing instructions.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37375-golden-state-medical-supply-recalls-50mg-tramadol-tablets-due-to. Based on FDA recall #D-0856-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0856-2020%22&limit=1).
Why it’s dangerous
The patient leaflets for the recalled tablets mention a 25mg dosing titration that requires using a scored 50mg tablet. However, the tablets are unscored, so patients might attempt to split them without proper scoring, which could lead to incorrect dosing.
Who’s affected
Patients prescribed 50mg Tramadol hydrochloride tablets by a doctor who received the recalled lots. Those who have the specific NDC numbers and expiration dates listed in the recall are most at risk.
How to tell if you have this one
Check for 100-count bottles (NDC 60429-588-01) or 500-count bottles (NDC 60429-588-05) with specific lot numbers and expiration dates listed in the recall. The tablets are unscored and labeled with incorrect dosing instructions.
- Brand
Golden State Medical Supply- Category
Drug
What to do — step by step
Check Product Details
Identify if your Tramadol tablets have the NDC numbers 60429-588-01 or 60429-588-05 and the listed lot numbers with specific expiration dates.
Questions people ask
Why is this recall happening?
The patient leaflets for the recalled tablets contain language relative to a 25mg dosing titration that requires using a scored 50mg tablet, but the tablets are unscored.
What should I do if I have these tablets?
Check the product details to see if your tablets are affected. If they are, contact your doctor or pharmacist for guidance on proper dosing.
Are there any safety risks from using these tablets?
The recall is due to incorrect dosing instructions, which could lead to improper dosing if someone tries to split the unscored tablets without scoring them.
Contact Golden State Medical Supply
We’ve drafted a message you can send Golden State Medical Supply to request your refund or repair — edit it as you like.
Subject: Recall D-0856-2020 — Golden State Medical Supply Golden State Medical Supply Hello, I own a Golden State Medical Supply that is covered by recall D-0856-2020 from Golden State Medical Supply. 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-0856-2020 (February 12, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0856-2020 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.