Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, potentially preventing proper product 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 medical device with a mechanical defect that could prevent proper assembly and use. Per the rubric, this is classified as High (3) because it is a risk-of-harm product where injury has not yet been reported.
Plain-English summary
Zimmer Biomet, Inc. is recalling 638 units of the Affixus Hip Fracture Nail, 130 DEG 9MM X 180MM. The recall affects Item No. 814509180, Lot No. 459290, with an expiration date of 05/17/2027. The product was 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 that have received this product should stop using it and contact Zimmer Biomet for instructions on returning the units. The source text does not report any illnesses or injuries associated with this recall.
The recalled product
- Product
- Affixus Hip Fracture Nail, 130 DEG 9MM X 180MM
- Manufacturer
- Zimmer Biomet, Inc.
- 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 (4)
- Item No. 814509180
- Lot No. 459290
- Exp. Date 05/17/2027
- (01)00887868038846 (17)270517 (10)459290
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.
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