Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center recalls PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL
Nephron recalls 5x10mL PF-Succinylcholine Chloride Injection due to incorrect or missing lot and expiration dates. This affects prescription-only injectable medication.
Lower-risk recall
Incorrect labeling: Incorrect or missing lot and/or exp date
Contact the company & request your remedy
What happened, in plain English
Nephron is recalling prescription-only succinylcholine injection vials that may have incorrect or missing lot and expiration dates. This could lead to medication errors if the wrong batch is used. Read more at govinfonow.com/recall/37816-nephron-pf-succinylcholine-chloride-injection-recall-incorrect-lot-exp-date.
Source Summary by GovInfoNow · govinfonow.com/recall/37816-nephron-pf-succinylcholine-chloride-injection-recall-incorrect-lot-exp-date · Updated October 5, 2026 · FDA enforcement record: FDA #D-0154-2020
Cite this page
“Nephron PF-Succinylcholine Chloride Injection Recall: Incorrect Lot/Exp Date Labeling.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37816-nephron-pf-succinylcholine-chloride-injection-recall-incorrect-lot-exp-date. Based on FDA recall #D-0154-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0154-2020%22&limit=1).
Why it’s dangerous
Incorrect labeling means the lot number or expiration date might be missing or wrong. This could cause medication errors if healthcare providers use the wrong batch of injection.
Who’s affected
Prescription patients receiving this specific injection from Nephron. Healthcare providers using the product in clinical settings are most at risk.
How to tell if you have this one
Check for the product name 'PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL)' in single-dose containers. Look for lot numbers SU9079A or SU9079B with expiration date 4/5/2020.
- Brand
Nephron- Category
Drug
What to do — step by step
Check Labeling
Verify the lot number and expiration date on the vial. If missing or incorrect, stop using it.
Questions people ask
Is this product safe to use?
The recall is for incorrect or missing lot and expiration dates. If labeling is correct, it may be safe, but the product should be checked against the listed lots.
What should I do if I have this product?
Check the lot number and expiration date. If they match SU9079A or SU9079B with expiration 4/5/2020, contact Nephron for instructions.
How can I confirm if my product is recalled?
Look for the lot numbers SU9079A or SU9079B with expiration date 4/5/2020 on the vial label.
Contact Nephron
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0154-2020 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0154-2020 from Nephron. 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-0154-2020 (October 21, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0154-2020 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.