Data Foundry

Medical device recalls 2019

Medtronic Adapter Percutaneous Pin — Class II medical device recall Z-0707-2020

Terminated recall by Medtronic Navigation, Inc., reported 2019-12-25, distributed nationwide. Under certain circumstances, the percutaneous pin adapter used with the StealthAir Frame Assembly may slightly

Recall numberZ-0707-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMedtronic Navigation, Inc., Louisville, CO, United States
Recall initiated2018-12-06
Classified2019-12-19
Reported by FDA2019-12-25
Terminated2020-12-17
DistributedNationwide (US)
Quantity1,297 percutaneous
UPC / GTIN / UDI-DI00643169529489, 00643169529533, 00643169540521, 00643169641006, 00763000054915, 00763000208462
Lot numbers150114, 150505, 150506, 150904, 151005, 151007, 160201, 160224, 160419, 160617, 160707, 170216, 180110, 180409
Model numbers9734752, 9734752-G02, 9734752K, 9735502, 9735502-G02

Product

Medtronic Adapter Percutaneous Pin, REF 9734752 (GTIN 00643169529489) and REF 9734752-G02 (GTIN 00763000054915), contained in the following kits: Upgrade Set Percutaneous Pin, REF 9735502 (GTIN 00643169529533) and REF 9735502-G02 (GTIN 00763000208462); Medtronic Adapter Percutaneous Pin Kit, REF 9734752K (GTIN 00643169540521); and Medtronic Adapter Percutaneous Pin Kit, REF 9734752K (GTIN 00643169641006) (Japan). The percutaneous pin adapter is a component of the StealthAir Frame Assembly.

Reason for recall

Under certain circumstances, the percutaneous pin adapter used with the StealthAir Frame Assembly may slightly rotate after surgical placement and not return to its original position, even when connections are tight and secure.

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-0707-2020. 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.