RecallHawk
Class II Recall

ACS Cath Lab Pack

American Contract Systems, Inc.

Summary

The FDA issued a Class II for ACS Cath Lab Pack by American Contract Systems, Inc.. Reason: Product was sterilized with a higher than specification EO concentration..

Details

Source

Device Recall

External ID

Z-1040-2022

Action Date

2022-05-18

Status

Ongoing

Category

device

Product Description

ACS Cath Lab Pack

Lot/Code Info: Model FTCL83K, Lot 982221 UDI: 00191072151360

Quantity Affected: 10 packs

Reason for Recall

Product was sterilized with a higher than specification EO concentration.

Distribution

US Nationwide distribution in the states of IL, MO, NE, and TX.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-03-22

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

American Contract Systems, Inc. has 188 FDA actions in our database, including 188 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 (American Contract Systems, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does American Contract Systems, Inc. have FDA actions?

American Contract Systems, Inc. has 188 FDA actions in our database, including 188 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-1040-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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