RecallHawk
Class II Recall

ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605

SCIENCE & BIO MATERIALS

Summary

The FDA issued a Class II for ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605 by SCIENCE & BIO MATERIALS. Reason: Mislabeled product..

Details

Source

Device Recall

External ID

Z-1361-2022

Action Date

2022-07-20

Status

Completed

Category

device

Product Description

ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605

Lot/Code Info: Product code: 110004605; Lot #: 190491, Use before 01/01/2022. GTIN 03760154006767

Quantity Affected: 72 units

Reason for Recall

Mislabeled product.

Distribution

US Nationwide distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-07

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

SCIENCE & BIO MATERIALS has 2 FDA actions in our database, including 2 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 (SCIENCE & BIO MATERIALS) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does SCIENCE & BIO MATERIALS have FDA actions?

SCIENCE & BIO MATERIALS has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-1361-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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