Pharmedium Services, LLC recalls morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL , For IV Use, Rx Only, Compounded by:
PharMEDium Services LLC recalls morphine sulfate injections with missing lot or expiration dates. Patients should contact their pharmacy for safe alternatives.
Lower-risk recall
Labeling: Incorrect or Missing Lot and/or Exp. Date
Contact the company & request your remedy
What happened, in plain English
PharMEDium Services LLC recalled morphine sulfate injections that may have missing or incorrect lot and expiration dates. This could lead to medication errors if the wrong batch is used. Read more at govinfonow.com/recall/41165-pharmedium-morphine-injection-recall-missing-lot-exp-date.
Source Summary by GovInfoNow · govinfonow.com/recall/41165-pharmedium-morphine-injection-recall-missing-lot-exp-date · Updated October 7, 2026 · FDA enforcement record: FDA #D-0131-2018
Cite this page
“PharMEDium morphine injection recall: Missing lot/exp date.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41165-pharmedium-morphine-injection-recall-missing-lot-exp-date. Based on FDA recall #D-0131-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0131-2018%22&limit=1).
Why it’s dangerous
Incorrect or missing lot and expiration dates could cause medication errors. Using the wrong batch might lead to incorrect dosing or ineffective treatment.
Who’s affected
Patients prescribed morphine injections by a healthcare provider who received this specific compounded product from PharMEDium Services LLC. Healthcare providers using this product for IV administration are most at risk.
How to tell if you have this one
Check for lot numbers starting with 172410028C or 172470030C and expiration dates of November 28, 2017 or December 4, 2017. This product was compounded by PharMEDium Services LLC in Cleveland, MS.
- Brand
PharMEDium- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Nationwide.
| Recall number | Product, codes & lots |
|---|---|
| D-0130-2018 | morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Volume 1 mg per mL (2 mg per 2 mL), For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-259-28; Lot: 172360026C; Exp. 11/23/2017 |
| D-0131-2018 | morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL , For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-455-78; Lot:172410028C; Exp. 11/28/2017 Lot: 172470030C; Exp. 12/04/2017 |
| D-0132-2018 | HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-165-78; Lot: 172410025C; Exp. 11/27/2017 |
What to do — step by step
Check Product Labels
Look for lot numbers starting with 172410028C or 172470030C and expiration dates of November 28, 2017 or December 4, 2017.
Questions people ask
Is this product safe to use?
The recall is due to missing or incorrect lot and expiration dates, which could lead to medication errors. Do not use this product if you cannot verify the lot and expiration dates.
How do I get a replacement?
The recall record does not specify a replacement process. Contact your pharmacy or healthcare provider for safe alternatives.
What should I do if I have this product?
Check the product labels for the specific lot numbers and expiration dates mentioned. If they are incorrect or missing, contact your healthcare provider immediately.
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-0131-2018 — PharMEDium PharMEDium Hello, I own a PharMEDium that is covered by recall D-0131-2018 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-0131-2018 (September 26, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0131-2018 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.