RecallHawk
Class II Recall

NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701

Stradis Medical, LLC dba Stradis Healthcare

Summary

The FDA issued a Class II for NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701 by Stradis Medical, LLC dba Stradis Healthcare. Reason: The sterile barrier may be compromised..

Details

Source

Device Recall

External ID

Z-1554-2022

Action Date

2022-08-24

Status

Ongoing

Category

device

Product Description

NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701

Lot/Code Info: SKU/Part Number: ZZ-0701; Lots: 22027483172 and 22131487071 UDI/DI: M752ZZ07010

Quantity Affected: 850 units

Reason for Recall

The sterile barrier may be compromised.

Distribution

US Nationwide distribution in the state of SC.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-07-25

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

Stradis Medical, LLC dba Stradis Healthcare has 93 FDA actions in our database, including 93 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 Medical, LLC dba 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 Medical, LLC dba Stradis Healthcare have FDA actions?

Stradis Medical, LLC dba Stradis Healthcare has 93 FDA actions in our database, including 93 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-1554-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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