3-D Matrix PuraSinus Nasal Hemostat Recall: Transport Box Hazard

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Contact the company & request your remedy

Recalling firm3-D Matrix, Inc.1234 Chestnut St Ste 205, N/A · Newton, MA 02464-1451

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

3-D Matrix is recalling PuraSinus Absorbable Nasal Hemostat with part number 651-006 because the shipping boxes weren't tested for safe transport. This could lead to damage during shipping, but the product itself isn't unsafe when used properly.

Why it’s dangerous

The shipping boxes weren't validated for safe transport, which could cause damage to the device during shipping. This doesn't affect the device's safety when used by medical professionals.

Who’s affected

Medical professionals who use this nasal hemostat device are likely affected. Patients using the device are at minimal risk as the hazard is only during shipping.

How to tell if you have this one

Check for part number 651-006 on the device. The lot number 19E30A50 is also associated with this recall.

Brand
3-D Matrix
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Part Number
Look for part number 651-006 on the device or its packaging.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

Yes, the product is safe for medical use. The recall is only about shipping boxes, not the device itself.

How do I know if I have the recalled product?

Check for part number 651-006 and lot number 19E30A50 on the device or its packaging.

What should I do if I have the recalled product?

The recall doesn't specify a remedy, so no action is needed beyond checking the part number.

Take action

Contact 3-D Matrix

We’ve drafted a message you can send 3-D Matrix to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0744-2022 — 3-D Matrix 3-D Matrix

Hello,

I own a 3-D Matrix that is covered by recall Z-0744-2022 from 3-D Matrix.

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-0744-2022 (December 2, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0744-2022 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.

3-D Matrix, Inc. recalls PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006

Lower-risk recall