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Terminated

Peregrine 20 GA Endo Ocular Adjustable Laser Probe

FDA Recall Z-2399-2010 · Posted 2010-09-11

Recalling FirmPeregrine Surgical Ltd
Recall StatusTerminated
Product CodeHQF
Date Initiated2010-07-19
Date Terminated2010-09-30
Product Quantity132 boxes

Reason for Recall

Product did not have proper 510(k) clearance

Firm Action

A recall letter is being sent to all affected accounts with instructions to return the recalled product to the recalling firm.

Root Cause

Other

Distribution Pattern

Product was distributed to hospitals and eye surgery centers in Florida, Maryland, Missouri, North Carolina, Ohio, Pennsylvania, Texas.

Official Source

View FDA Recall →

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

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