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

Recall Z-1441-2017 — RTI Biologics BioSet IC RT Paste 2 cc Filler, bone void, calcium compound. Use in dental, spine and orthopedic applications

U.S. FDA — Device Enforcement · United States · 2017-01-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1441-2017
Date of alert
2017-01-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
RTI Surgical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
30303308
Reported risk: Incorrect instructions for use (IFU) included.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.