Data Foundry

Medical device recalls 2018

Model #: CG8900 — Class II medical device recall Z-0622-2018

Terminated recall by Medtronic Neurosurgery, reported 2018-02-21, distributed in GU. Medtronic is initiating a voluntary recall because the products identified above did not adequately demonstrat

Recall numberZ-0622-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMedtronic Neurosurgery, Goleta, CA, United States
Recall initiated2017-12-20
Classified2018-02-15
Reported by FDA2018-02-21
Terminated2023-12-08
DistributedGU
Countries outside the USAE, AU, CA, CH, CY, DE, DZ, EG, ES, GB, GH, GR, ID, IR, IS, IT, JO, NZ, PL, PT, SA, SE, SG, TN, TR, ZA
Quantity27,432
Lot numbersD80412, D80413, D84100, D84101, E00008, E00009, E00983, E00984, E03049, E03050, E03716, E03717, E05233, E05806, E05807, E05810, E07257, E07258, E09117, E09145, E09146, E09149, E09239, E11242, E11243, E11244, E11706, E12011, E12012, E13574, E14782, E14784, E14896, E14898, E15195, E15197, E19181, E19182, E19183, E19184 and 31 more
Model numbersCG8900, CG8901, CG8901A

Product

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)

Reason for recall

Medtronic is initiating a voluntary recall because the products identified above did not adequately demonstrate acceptable packaging performance to current standards.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0622-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.