Pharmedium Services, LLC recalls Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP (0.2 units per mL), Rx only, PharMEDium
PharMEDium Services recalls vasopressin injection due to cGMP deviations. This medication is prescription-only and may pose risks if used improperly.
Recall notice
cGMP deviations
Contact the company & request your remedy
What happened, in plain English
PharMEDium Services recalls a specific vasopressin injection product because of manufacturing quality issues. This recall affects prescription-only medication that could have safety risks if used without proper quality control. Read more at govinfonow.com/recall/40624-pharmedium-vasopressin-injection-recall-cpg-deviations-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/40624-pharmedium-vasopressin-injection-recall-cpg-deviations-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0632-2018
Cite this page
“PharMEDium Vasopressin Injection Recall: CPG Deviations Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40624-pharmedium-vasopressin-injection-recall-cpg-deviations-risk. Based on FDA recall #D-0632-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0632-2018%22&limit=1).
Why it’s dangerous
The recall is due to cGMP deviations, which are manufacturing quality issues that could affect the safety and effectiveness of the medication. These deviations may lead to improper drug composition or contamination risks.
Who’s affected
Prescription patients using this specific vasopressin injection product are affected. Healthcare providers who dispense the medication may also be impacted.
How to tell if you have this one
Check for the product name 'Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP (0.2 units per mL)' and the lot number 180660057S with an expiration date of 6/5/2018.
- Brand
PharMEDium- Category
Drug
What to do — step by step
Check Product Details
Verify the lot number 180660057S and expiration date 6/5/2018 on the product label.
Questions people ask
Is this product safe to use?
The recall indicates potential manufacturing quality issues, so it is not recommended for use until the recall is addressed.
How do I know if I have the recalled product?
Check for the lot number 180660057S and expiration date 6/5/2018 on the product label.
What should I do if I have this product?
The recall does not specify a remedy, so contact PharMEDium Services for guidance.
Contact PharMEDium
We’ve drafted a message you can send PharMEDium to request your refund or repair — edit it as you like.
Subject: Recall D-0632-2018 — PharMEDium PharMEDium Hello, I own a PharMEDium that is covered by recall D-0632-2018 from PharMEDium. 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-0632-2018 (April 10, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0632-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.