RecallHawk
Class II Recall

Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040

Cardinal Health

Summary

The FDA issued a Class II for Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040 by Cardinal Health. Reason: Potential for open packaging seals compromising the sterility of the surgical gowns.

Details

Source

Device Recall

External ID

Z-0373-2022

Action Date

2021-12-22

Status

Ongoing

Category

device

Product Description

Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040

Lot/Code Info: Lot Numbers: 20MEQ001 21AEQ00 21BEQ001 21BEQ002 21BEQ003 21CEQ001 21DEQ001 21DEQ002 21EEQ001 21EEQ002 21FEQ001 21FEQ002 21GEQ001 21HEQ001 21HEQ002 21JEQ001 21JEQ002. UDI: 50192253018989 (cs) 10192253018981 (ea)

Quantity Affected: 146,939 units

Reason for Recall

Potential for open packaging seals compromising the sterility of the surgical gowns

Distribution

Worldwide distribution - US Nationwide and the countries of Chile, Thailand, Canada, Israel, LATAM Dist.Qatar, LATAM/Panama, LATAM/Mexico, LATAM/Colombia, LATAM/Costa Rica.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-11-02

Company

Cardinal Health

Waukegan, IL

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 193 device recalls issued in the same week, part of 403 device-related FDA actions this month.

Cardinal Health has 20 FDA actions in our database, including 20 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 (Cardinal Health) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Cardinal Health have FDA actions?

Cardinal Health has 20 FDA actions in our database, including 20 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-0373-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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