The Recall Desk
HighFDA (Devices)·Z-0461-2018·Announced 2018-02-07

Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.

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 involves a high-risk medical device where a mechanical defect could prevent proper assembly, posing a risk of harm, but the source text does not report any specific injuries or illnesses.

Plain-English summary

Zimmer Biomet, Inc. is recalling 638 units of the Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM (Item No. 814309460). The affected units were distributed nationwide in the United States, as well as in Portugal and the Netherlands.

The recall was initiated after it was detected during a rework process for a previous field action that the set screw and sleeve assembly, which are designed to have an interference fit, were no longer in their installed location. This defect could prevent the product from being properly assembled with the mating screw and targeting jig.

Healthcare providers and facilities should stop using the affected devices and contact Zimmer Biomet for instructions on how to return or replace the units. Patients who have already received these implants should contact their healthcare provider to discuss the potential impact on their specific medical situation.

The recalled product

Product
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM
Affected units
638

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)

  • Item No. 814309460

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 65 recalled by Zimmer Biomet, Inc. 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 65 products in this recall →