The Recall Desk
HighFDA (Devices)·Z-2709-2018·Announced 2018-08-15

Howmedica Recalls rHead Recon Extended Stem Orthopedic Implants

Howmedica Osteonics Corp. is recalling 19 rHead Recon Extended Stem Size 3 orthopedic implants due to a higher-than-expected revision rate.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II. The hazard involves a medical device that may not perform as expected, leading to a higher revision rate, which fits the criteria for a risk-of-harm product where specific injury reports are not detailed in the source text.

Plain-English summary

Howmedica Osteonics Corp. is recalling 19 units of the rHead Recon Extended Stem Size 3. This product is an orthopedic implant used for the replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.

The recall was initiated because a literature review identified that the revision rate for this device is higher than that of other proximal radial head replacement devices. The source text notes that the product may not perform at the expected level post-surgery.

The affected units were distributed nationwide in the United States. The source text does not specify specific hospitals or patients affected, nor does it report any specific injuries or illnesses associated with the recall.

The recalled product

Product
rHead Recon Extended Stem Size 3. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.
Affected units
19

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • 410-0302

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 70 recalled by Howmedica Osteonics Corp. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 70 products in this recall →