C.R. Bard Foley Catheter Recall: Incorrect Retainer Cap Print Hazard

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Recalling firmC.R. Bard, Inc.8195 Industrial Blvd NE, N/A · Covington, GA 30014-1497

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✎ GovInfoNow plain-language explainer

What happened, in plain English

C.R. Bard is recalling a specific type of continuous irrigation Foley catheter because the retainer cap print is incorrect. This could lead to improper use if the catheter is not secured properly.

Why it’s dangerous

The incorrect retainer cap print may cause the catheter to become loose or dislodged during use. This could lead to improper catheter placement or potential injury if the catheter is not secured correctly.

Who’s affected

Patients who use the recalled catheter model are affected. Healthcare providers and caregivers who handle these catheters may also be at risk if they use the incorrect model.

How to tell if you have this one

Check for the model number 01267522 on the catheter packaging. Lot numbers NGBR0383 and NGBR2129 are associated with the recalled units.

Brand
C.R. Bard
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Model Number
Look for the model number 01267522 on the catheter packaging or label.

✎ GovInfoNow

Questions people ask

What is the specific model of catheter being recalled?

The recalled model is Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522).

What lot numbers are affected by this recall?

Lot numbers NGBR0383 and NGBR2129 are associated with the recalled units.

Is there a remedy for this recall?

The recall record does not specify a remedy.

Take action

Contact C.R. Bard

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

✉️ Open in email

Subject: Recall Z-2064-2018 — C.R. Bard C.R. Bard

Hello,

I own a C.R. Bard that is covered by recall Z-2064-2018 from C.R. Bard.

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-2064-2018 (December 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2064-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 31, 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.

C.R. Bard, Inc. recalls Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)

Lower-risk recall