Fluorescence Imaging Procedure Kits used with the da Vinci Si and Xi… — Class II medical device recall Z-2782-2015
Terminated recall by Intuitive Surgical, Inc., reported 2015-09-23, distributed nationwide. B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit may experience damage to the sterile
| Recall number | Z-2782-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intuitive Surgical, Inc., Sunnyvale, CA, United States |
| Recall initiated | 2015-09-09 |
| Classified | 2015-09-17 |
| Reported by FDA | 2015-09-23 |
| Terminated | 2015-11-02 |
| Distributed | Nationwide (US) |
| Quantity | 1,200 kits |
| Reason classes | sterility |
| Lot numbers | NQ141201, NQ141502, NQ142201, NQ142901, NQ143201, NQ143301, NQ143501, NQ143502, NQ143601, NQ143602, NQ143803, NQ143901, NQ143902, NQ144001, NQ144502, NQ144801, NQ144901, NQ145201, NQ145202, NQ145301, NQ150301, NQ150501, NQ150601, NQ150602, NQ150701, NQ150702, NQ150703, NQ150801, NQ150802, NQ150901, NQ151001, NQ151002, NQ151101 |
| Model numbers | 950156-01, 950156-02, 950156-03 |
Product
Fluorescence Imaging Procedure Kits used with the da Vinci Si and Xi Surgical Systems; Model numbers: 950156-01, 950156-02, 950156-03. Product Usage: General and plastic surgery: The da Vinci Firefly Imaging system is intended to provide real-time endoscopic visible and near-infrared fluorescence imaging.
Reason for recall
B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit may experience damage to the sterile packaging during shipping. The damage can result in tears to the packaging and has the potential to cause a breach in sterility of the supplied stopcocks.
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-2782-2015. 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.