RecallHawk
Class II Recall

Surgical Suture Kit

Stradis Healthcare

Summary

The FDA issued a Class II for Surgical Suture Kit by Stradis Healthcare. Reason: There is uncertainty about the integrity of the methods used to ensure the sterile barrier integrity..

Details

Source

Device Recall

External ID

Z-1132-2022

Action Date

2022-06-01

Status

Ongoing

Category

device

Product Description

Surgical Suture Kit

Lot/Code Info: Part Number: ZZ-0958; Primary DI Number: M752ZZ09580; Lot Numbers: 213639474, 212957814, 212675717

Quantity Affected: 7340 units

Reason for Recall

There is uncertainty about the integrity of the methods used to ensure the sterile barrier integrity.

Distribution

US Distribution to NC.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-22

Company

Stradis Healthcare

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

Stradis Healthcare 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 (Stradis Healthcare) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Stradis Healthcare have FDA actions?

Stradis Healthcare 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-1132-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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