Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1233-2014 — ENDOBON XENOGRAFT GRANULES 0.5 ML (Bovine bone substitute) Endobon is a bone substitute of bovine origin formed from ceramised bone for implantation or transplantation when bone is lost due to trauma or requested during reconstructive surgery.

U.S. FDA — Device Enforcement · United States · 2013-10-03 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1233-2014
Date of alert: 2013-10-03
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Biomet 3i, LLC
Product category: device
Product type: Devices

Reported risk: Individual pieces of a batch of Biomet's Endobon Xenograft Granules 0.5 ML (Bovine Bone substitute) may have an incorrect label with the wrong batch number.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Recall Z-1233-2014 — ENDOBON XENOGRAFT GRANULES 0.5 ML (Bovine bone substitute) Endobon is a bone substitute of bovine origin formed from ceramised bone for implantation or transplantation when bone is lost due to trauma or requested during reconstructive surgery.

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