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Terminated

MurphyScope, Curved, Mallaeble, Catalog # 2125-163

FDA Recall Z-0616-05 · Posted 2005-03-12

Recalling FirmMedtronic Neurosurgery
Recall StatusTerminated
Product CodeGWG
Date Initiated2005-02-28
Date Terminated2005-07-12
Product Quantity2

Reason for Recall

Products are mislabeled.

Firm Action

Recall letters were sent to customers on 2/28/05 requesting return for replacement.

Root Cause

Process control

Distribution Pattern

NJ and India.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K010341MEDTRONIC PS MEDICAL MURPHYSCOPE, MODELS 2125-032, 2125033,2125-042, 2125-043, 2125-157, 2125-158,2125-161 2125-162,,Medtronic PS Medical · 2001-04-20

Official Source

View FDA Recall →

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

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