Monoject 20mL Syringe Recall: Compatibility Issues with Infusion Pumps

Take action

Contact the company & request your remedy

Recalling firmCardinal Health 200, LLC3651 Birchwood Dr, N/A · Waukegan, IL 60085-8337

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Cardinal Health is recalling Monoject 20 mL syringes with Luer-Lock tips because they can cause recognition and compatibility problems with infusion pumps. This could lead to improper medication delivery if used with certain pumps.

Why it’s dangerous

These syringes may not work correctly with certain infusion pumps, potentially causing medication delivery errors. The issue stems from recognition and compatibility problems between the syringe and pump systems.

Who’s affected

People who use these syringes for medical injections, particularly those with infusion pumps, are most at risk. The recall affects specific lot numbers produced between 2019 and 2023.

How to tell if you have this one

Check for lot numbers 221201 through 230206 on the syringe packaging. The product code 1182000777 and UDI/DI numbers 10192253034677 (syringe), 10192253034674 (box), and 10192253034675 (case) are also indicators.

Brand
Cardinal Health
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Syringe Lot Number
Look for lot numbers 221201 through 230206 on the syringe packaging.
Contact Manufacturer
Reach out to Cardinal Health 200, LLC for further assistance if you have the recalled syringes.

✎ GovInfoNow

Questions people ask

Why is this syringe being recalled?

The syringes have demonstrated recognition and compatibility issues with certain infusion pumps, which could lead to medication delivery errors.

What lot numbers are affected?

Lot numbers 221201 through 230206 are affected.

How can I tell if I have the recalled syringe?

Check for lot numbers 221201 through 230206 on the syringe packaging or look for the product code 1182000777 and UDI/DI numbers 10192253034677 (syringe), 10192253034674 (box), and 10192253034675 (case).

Take action

Contact Cardinal Health

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

✉️ Open in email

Subject: Recall Z-0148-2024 — Cardinal Health Cardinal Health

Hello,

I own a Cardinal Health that is covered by recall Z-0148-2024 from Cardinal Health.

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

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.

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 #Z-0148-2024 (September 20, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0148-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

Cardinal Health 200, LLC recalls Monoject 20 mL Syringe Luer-Lock Tip Soft Pack

Use caution until it’s fixed