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Terminated

MicroSTAAR Injector, MSI-PF Packed ten per box.

FDA Recall Z-0957-04 · Posted 2004-07-20

Recalling FirmStaar Surgical Co Inc
Recall StatusTerminated
Product CodeKYB
Date Initiated2004-04-21
Date Terminated2012-07-26
Product Quantity124 boxes, 10 per box.

Reason for Recall

Cracking of the distal end of the injector occurs during locking of the cartridge into the nose cone of the injector.

Firm Action

Recall will be implemented by visits by company representatives.

Root Cause

Other

Distribution Pattern

Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K980696FOAM TIP INJECTORStaar Surgical Co. · 1998-09-11

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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