Baxter DISCPAC Syringe Tip Caps Recall: Sterile Packaging Risk

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Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter is recalling pink 100-pack syringe tip caps that may not maintain sterile packaging. This could lead to contamination if the caps are used in medical procedures. The recall affects all units sold with the reference number REF H938676100.

Why it’s dangerous

The packaging may fail to keep the tip caps sterile, which could lead to contamination during medical procedures. This risk is specific to the product's design and usage in healthcare settings where sterility is critical.

Who’s affected

Healthcare professionals and patients using Baxter DISCPAC syringe tip caps for medical procedures are likely affected. Those handling the product in clinical settings face the highest risk due to potential contamination.

How to tell if you have this one

Check for the pink 100-pack syringe tip caps with reference number REF H938676100. All lots of this product are affected, including those with UDI 00085412479859.

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the reference number REF H938676100 on the packaging to confirm if your product is affected.

✎ GovInfoNow

Questions people ask

Is there a remedy for this recall?

The official notice does not specify any remedy for this recall.

Which lots of the product are affected?

All lots of the pink 100-pack syringe tip caps with reference number REF H938676100 are affected.

How can I tell if my product is part of this recall?

Check for the reference number REF H938676100 on the packaging. All lots with this reference are affected.

Take action

Contact Baxter

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

✉️ Open in email

Subject: Recall Z-1580-2022 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-1580-2022 from Baxter.

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-1580-2022 (July 22, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1580-2022 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.

Baxter Healthcare Corporation recalls Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Pink, 100 pack, REF H938676100

Recall notice