FDAClass IIFebruary 23, 2022

Exeter V40 Cemented Hip recall: Labeling Error

Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440

Why was Exeter V40 Cemented Hip recalled?

There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

GTIN: 04546540153296; Lot G7900352

Product
Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
Recalling firm
Howmedica Osteonics Corp.
Quantity
58 devices
Distribution
The product was distributed to the following US states: MI
Recall date
February 23, 2022
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls