Skip to content
Drug recall · FDA · Published June 29, 2018

SCA Pharmaceuticals recalls Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total

SCA Pharmaceuticals recalls specific lots of Buffered Lidocaine 1% injection for local anesthesia due to potential stability problems affecting expiration dates. Consumers should check their lot numbers and contact the manufacturer for details.

🇺🇸 FDA recall #D-0918-2018DrugSCA Pharmaceuticals ›
Take action

Contact the company & request your remedy

Recalling firmSCA Pharmaceuticals8821 Knoedl Ct · Little Rock, AR 72205-4600
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

SCA Pharmaceuticals has recalled certain lots of Buffered Lidocaine 1% injection for local anesthesia because the drug may lose potency before the expiration date. This means the medication might not work as intended if used after the recalled dates. Read more at govinfonow.com/recall/40388-sca-pharmaceuticals-recalls-lidocaine-injection-due-to-stability-issues.

Source Summary by GovInfoNow · govinfonow.com/recall/40388-sca-pharmaceuticals-recalls-lidocaine-injection-due-to-stability-issues · Updated October 6, 2026 · FDA enforcement record: FDA #D-0918-2018

Cite this page

“SCA Pharmaceuticals Recalls Lidocaine Injection Due to Stability Issues.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/40388-sca-pharmaceuticals-recalls-lidocaine-injection-due-to-stability-issues. Based on FDA recall #D-0918-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0918-2018%22&limit=1).

Why it’s dangerous

The stability data for the medication does not support the current expiration dating of 55 days after compounding. This means the drug could become less effective over time, potentially leading to reduced pain relief during procedures.

Who’s affected

Healthcare professionals and patients who have the recalled lots of Buffered Lidocaine 1% injection for local anesthesia. Those using the medication for procedures like minor surgeries or dental work are most at risk.

How to tell if you have this one

Check the lot number on the label, which includes dates like 20180507@21, 20180511@9, etc. The product is only available by prescription and has specific expiration dates listed in the recall notice.

  • Brand
    SCA Pharmaceuticals
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Lot Number

    Look for the lot number on the label, such as 20180507@21 or 20180511@9.

✎ GovInfoNow

Questions people ask

What is the specific product being recalled?

Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total, available by prescription.

How can I check if I have the recalled product?

Check the lot number on the label, which includes dates like 20180507@21, 20180511@9, etc. The product is only available by prescription.

What should I do if I have the recalled product?

The recall does not specify a remedy, so contact SCA Pharmaceuticals at 877-550-5059 for further instructions.

Take action

Contact SCA Pharmaceuticals

We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.

Subject: Recall D-0918-2018 — SCA Pharmaceuticals SCA Pharmaceuticals

Hello,

I own a SCA Pharmaceuticals that is covered by recall D-0918-2018 from SCA Pharmaceuticals.

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.

Similar recalls

Keep exploring

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Comments are reviewed before they appear. No links, ads, or personal attacks — those get removed.

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-0918-2018 (June 29, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0918-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA