RecallHawk
Class II Recall

Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

FX SHOULDER

Summary

The FDA issued a Class II for Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210 by FX SHOULDER. Reason: Centered glenosphere box may contain an eccentric glenosphere..

Details

Source

Device Recall

External ID

Z-0843-2024

Action Date

2024-02-07

Status

Ongoing

Category

device

Product Description

Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

Lot/Code Info: UDI-DI: 03701037309551, Lot: U0191

Quantity Affected: 4

Reason for Recall

Centered glenosphere box may contain an eccentric glenosphere.

Distribution

US Nationwide distribution in the state of NJ.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-08

Company

FX SHOULDER

Dallas, TX

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

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

How often does FX SHOULDER have FDA actions?

This is the only FDA action we have on record for FX SHOULDER in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-0843-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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