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

Recall Z-2074-2015 — Abutment Retrieval Instrument Zirconia CC RP/WP, Article No. 37882 and Abutment Retrieval Kit, Article No. 37508 (Article No. 37882 was assembled in this kit). Used to remove a zirconia abutment if the abutment is stuck in the implant connection due to a tight seat. Endosseous dental implant instr

U.S. FDA — Device Enforcement · United States · 2015-06-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2074-2015
Date of alert: 2015-06-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Nobel Biocare Usa Llc
Product category: device
Product type: Devices

Reported risk: One dimension of the affected instrument is incorrect. Therefore this instrument cannot be used to remove the metal adapter as intended.

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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.

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