Cardinal Health Monoject Blunt Cannula Recall: Sterility Risk

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Contact the company & request your remedy

Recalling firmCardinal Health 200, LLC15 Hampshire St Bldg 5, N/A · Mansfield, MA 02048-1113

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Cardinal Health is recalling certain Monoject Blunt Cannula syringes because a manufacturing defect might compromise their sterility barrier. This could lead to infections if the product is used without proper sterility.

Why it’s dangerous

The syringes have a manufacturing defect that could compromise the sterility barrier. This means the product might not be sterile when used, increasing the risk of infection during injections.

Who’s affected

People who own or use the recalled Monoject Blunt Cannula syringes (19G x 1-1/2" with item code 8881202355) are affected. Healthcare professionals and patients using these syringes for injections are most at risk.

How to tell if you have this one

Check for the item code 8881202355 on the syringe packaging. The affected lots are 905617, 905618, 905619, 905620, 907004, and 907005.

Brand
Cardinal Health
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for the lot numbers 905617, 905618, 905619, 905620, 907004, or 907005 on the syringe packaging.

✎ GovInfoNow

Questions people ask

What is the item code for the recalled syringes?

The item code is 8881202355.

Which lot numbers are affected?

The affected lot numbers are 905617, 905618, 905619, 905620, 907004, and 907005.

How can I tell if my syringe is recalled?

Check the syringe packaging for the item code 8881202355 and the affected lot numbers listed above.

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-2050-2019 — Cardinal Health Cardinal Health

Hello,

I own a Cardinal Health that is covered by recall Z-2050-2019 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.

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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 #Z-2050-2019 (April 30, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2050-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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 Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355

Lower-risk recall