The Recall Desk
HighFDA (Devices)·Z-3109-2018·Announced 2018-09-19

Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Malfunction

Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

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 functional defect that could compromise the stability of a hip fracture fixation. 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 5,947 units of the Affixus Hip Fracture Nail Right 130° 9 mm x 260 mm (Item Number: 814509260). The recall was initiated because the set screw is not able to advance or reverse from the original position in the nail.

The affected products were distributed to 38 US states and Puerto Rico, as well as to Chile, Ecuador, Japan, and the Netherlands. The specific states included in the distribution are AL, AR, AZ, CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WY.

Healthcare providers and patients should contact Zimmer Biomet for instructions on how to proceed with the recall. The source text does not report any illnesses or injuries associated with this defect.

The recalled product

Product
Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 260 mm, Item Number: 814509260
Affected units
5,947

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)

  • 813650

Distribution

Part of a larger recall action

This product is one of 129 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 129 products in this recall →