NA CM8902Recalls & reported problems

Medtronic Ps Medical, Inc. · MAGAZINE CM8902 RANEY CLIP GUN 5PK · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports: 0
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

1 other recall cover devices cleared under the same FDA submission (K050044); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

May 3, 2018Terminated
The packaging sterile barrier does not comply with the applicable packaging standard for terminally sterilized medical devices. While the Instructions for Use (IFU) state Do not use if package has been previously opened or damaged , it is possible that the seal breach may go undetected by the user's naked eye.
Z-3212-2018 · Root cause: Under Investigation by firm · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K050044. One submission often covers many models, so check the product and lot details in each record.

Z-0622-2018 · Dec 20, 2017 · Terminated
Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model #: CG8901, Medtronic Clip Gun Scalp Clip Kit (Qty 10); Model #: CG8901A, Medtronic Clip Gun Applicator (Qty 10)

Device details

UDI-DI	`20643169647200`
Brand	NA
Model	CM8902
Company	Medtronic Ps Medical, Inc.
Product code	HBO · CLIP, SCALP
Class	Class 2
FDA submission	K050044
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Nov 15, 2023

Device type (GMDN): Scalp clip applier, single-use

A hand-held, manually-operated, surgical instrument used for the application (the attachment) of nonimplantable, single-use scalp clips to the margins of a scalp wound/incision during a surgical intervention on the cranium/scalp. Often referred to as a clip gun, it has a pistol-like design and holds an exchangeable, preloaded cassette of scalp clips that are fired into the scalp tissue, with the pull of a trigger, to approximate the margins of the wound/incision until it heals. This is a single-use device.

Other CLIP, SCALP devices

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1 recall4 reports
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2 reports
CODMAN 20-1037
Cerenovus, Inc. · CLIP, SCALP
2 reports
AESCULAP FF013P
Aesculap AG · CLIP, SCALP
1 report
CODMAN® 201038
Integra Lifesciences Production Corporation · CLIP, SCALP
1 report

All CLIP, SCALP devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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