AVID Medical recalls thoracoscopy basin kits with discoloration issue

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Contact the company & request your remedy

Recalling firmAVID Medical, Inc.9000 Westmont Dr, N/A · Toano, VA 23168-9351

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

AVID Medical is recalling certain thoracoscopy basin kits because resterilization caused discoloration. This issue doesn't pose a safety risk but may affect the kit's appearance and functionality.

Why it’s dangerous

The visualization system in the kits was resterilized incorrectly, leading to discoloration. This discoloration does not cause injury or malfunction but may impact the kit's appearance and usability.

Who’s affected

Medical professionals using the recalled thoracoscopy basin kits for procedures. Those with the specific model numbers and lot numbers listed are most at risk of receiving a discolored kit.

How to tell if you have this one

Check for model numbers NIHB0022-09, NIHB0022-11, or NIHB0022-12 on the kit. Also look for lot numbers 1580032, 1590461, 1590463, 1604743, 1613180, 1613182, 1618989, or 1641040.

Brand
AVID Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Model
Identify the model number on the kit to see if it matches NIHB0022-09, NIHB0022-11, or NIHB0022-12.
Check Kit Lot
Verify the lot number against the listed numbers: 1580032, 1590461, 1590463, 1604743, 1613180, 1613182, 1618989, or 1641040.

✎ GovInfoNow

Questions people ask

Why was the visualization system discolorated?

The visualization system was inadvertently resterilized in the kits, causing discoloration.

Do I need to stop using the kit?

No, the discoloration does not pose a safety risk, so you can continue using the kit.

How can I tell if my kit is affected?

Check for model numbers NIHB0022-09, NIHB0022-11, or NIHB0022-12 and lot numbers 1580032, 1590461, 1590463, 1604743, 1613180, 1613182, 1618989, or 1641040.

Take action

Contact AVID Medical

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

✉️ Open in email

Subject: Recall Z-2258-2025 — AVID Medical AVID Medical

Hello,

I own a AVID Medical that is covered by recall Z-2258-2025 from AVID Medical.

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-2258-2025 (June 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2258-2025 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.

AVID Medical, Inc. recalls MAJOR THORACOSCOPY BASIN. Medical convenience kit.

Lower-risk recall