FDAClass IIAugust 17, 2022

Corin Metafix HIP Stem recall

Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103

Why was Corin Metafix HIP Stem recalled?

One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI (01) 0 505563 89123 0 (10) 485630 (17) 261114, Lot Number 485630

Product
Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
Recalling firm
Corin Ltd
Quantity
5 devices
Distribution
US Nationwide distribution in the states of OK, TX, FL.
Recall date
August 17, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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