RecallHawk
Class II Recall

CT DAVINCI. Medical convenience kit.

AVID Medical, Inc.

Summary

The FDA issued a Class II for CT DAVINCI. Medical convenience kit. by AVID Medical, Inc.. Reason: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration..

Details

Source

Device Recall

External ID

Z-2242-2025

Action Date

2025-08-13

Status

Ongoing

Category

device

Product Description

CT DAVINCI. Medical convenience kit.

Lot/Code Info: Model No. WRNM089; UDI: 10809160432525; Kit Lot No. 1627141.

Quantity Affected: 12 units

Reason for Recall

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Distribution

Domestic: CA, IL, MD, OH, PA, TX, WA.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-06-11

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 172 device recalls issued in the same week, part of 403 device-related FDA actions this month.

AVID Medical, Inc. has 125 FDA actions in our database, including 125 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (AVID Medical, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AVID Medical, Inc. have FDA actions?

AVID Medical, Inc. has 125 FDA actions in our database, including 125 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-2242-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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