B. Braun Y-Type Blood Set Recall: Leakage Risk at Blood Filters

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Contact the company & request your remedy

Recalling firmB. Braun Medical, Inc.901 Marcon Blvd, N/A · Allentown, PA 18109-9512

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

B. Braun is recalling Y-Type Blood Sets with catalog number 490293 because they may leak at the joint between blood filters and tubing. This could lead to blood loss or contamination during medical procedures.

Why it’s dangerous

The blood filters and tubing may leak at their connection point, potentially causing blood loss or contamination during medical procedures. This could happen if the set is used improperly or if the joint becomes damaged.

Who’s affected

Healthcare professionals and patients using the Y-Type Blood Set with catalog number 490293. Those using the product for blood transfusions or procedures are most at risk.

How to tell if you have this one

Check for catalog number 490293 on the blood set packaging. The product was sold with lot number 61681734 and expired May 31, 2022.

Brand
B. Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for catalog number 490293 on the blood set packaging or label.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates a potential leakage risk, so it is not recommended for use until the remedy is applied. However, the remedy is not specified in the record.

What should I do if I have this product?

The recall record does not specify a remedy, so no action is required beyond checking the product details.

When was this product sold?

The product was sold with lot number 61681734 and expired May 31, 2022.

Take action

Contact B. Braun

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

✉️ Open in email

Subject: Recall Z-0936-2020 — B. Braun B. Braun

Hello,

I own a B. Braun that is covered by recall Z-0936-2020 from B. Braun.

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-0936-2020 (November 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0936-2020 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.

B. Braun Medical, Inc. recalls Y-Type Blood Set, Catalog Number 490293

Lower-risk recall