Z-0615-05

MurphyScope, Bayonet, Malleable, Catalog # 2121-157

Name: Z-0615-05 MurphyScope, Bayonet, Malleable, Catalog # 2121-157
Creator: Medtronic Neurosurgery
Published: 2005-02-28
License: https://open.fda.gov/license/

Medtronic Neurosurgery / initiated 2005-02-28 / Terminated / root cause: manufacturing process

FDA source

Medtronic Neurosurgery began a recall of MurphyScope, Bayonet, Malleable, Catalog # 2121-157 on 2005-02-28. The reason FDA records is "Products are mislabeled". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0615-05
Status: Terminated
Initiated: 2005-02-28
Posted: 2005-03-12
Terminated: 2005-07-12
Recalling firm: Medtronic Neurosurgery
Product: MurphyScope, Bayonet, Malleable, Catalog # 2121-157
Product code: GWG Endoscope, Neurological
Reason for recall: Products are mislabeled.
Root cause tag: manufacturing process
FDA root cause: Process control
Action: Recall letters were sent to customers on 2/28/05 requesting return for replacement.
Quantity in commerce: 2
Distribution: NJ and India.
Product codes and lots: Lot A52300

Product code GWG

K010341Class IIMedtronic Ps Medical Murphyscope, Models 2125-032, 2125033,2125-042, 2125-043, 2125-157, 2125-158,2125-161 2125-162,,Medtronic PS Medical / cleared 2001-04-20

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)