RecallRadar

FDA Device recall Z-0092-2027

DAVINCI TRUCUSTOM BUNDLE

On 2026-10-14 the FDA classified a Class II recall of DAVINCI TRUCUSTOM BUNDLE by Avid Medical, citing product may be potentially contaminated with a lubricant used during the manufacturing process.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0092-2027
ClassificationClass II
Statusongoing
Initiated2026-08-10
Published2026-10-14
Last updated2026-10-21 05:30 UTC
CompanyAvid Medical
DistributionUS

Product

DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;

Reason

Product may be potentially contaminated with a lubricant used during the manufacturing process.

Identifiers

code_info
1. Model/Item Number (Kit): SAMM064-27; UDI-DI: 10809160439708; Kit Lot Numbers: 1657586, 1658104, 1671251; 2. Model/I…1. Model/Item Number (Kit): SAMM064-27; UDI-DI: 10809160439708; Kit Lot Numbers: 1657586, 1658104, 1671251; 2. Model/Item Number (Kit): SAMM064-28; UDI-DI: 10809160516201; Kit Lot Numbers: 1698700; Recalled Supplier Component (in kit): A303416A; Recalled Supplier Lot Number (in kit): NGKU1749, NGKV0359;

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-21 05:30 UTC. Current status: ongoing.

Other recalls by Avid Medical

All Avid Medical recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0092-2027%22

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