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

Recall Z-1153-2014 — Treatment packs used on the VisuMax Laser Keratome. Size M Manufactured by Carl Zeiss Meditec AG, Jena, Germany. The VisuMax Laser Keratome is indicated for the following: In the creation of a corneal flap in patients undergoing LASIK surgery or other treatment requiring lamellar resection o

U.S. FDA — Device Enforcement · Germany · 2014-02-03 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1153-2014
Date of alert: 2014-02-03
Country / jurisdiction: Germany
Risk level: Class II
Risk type: recall
Brand: Carl Zeiss Meditec AG
Product category: device
Product type: Devices

Reported risk: Carl Zeiss Treatment pack, lot number M 130010, size M, may actually contain size S.

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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