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

Recall Z-1788-2014 — Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device is to be used as a dental restorative material in the treatment of dental caries.

U.S. FDA — Device Enforcement · United States · 2014-05-29 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1788-2014
Date of alert: 2014-05-29
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Kerr Corporation
Product category: device
Product type: Devices

Reported risk: Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number 29948, Lot Number 3-1294), because it may set faster than specified in the Directions for Use.

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.

Recall Z-1788-2014 — Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device is to be used as a dental restorative material in the treatment of dental caries.

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