BARDIA¿ 60cc Piston Irrigation Syringe — Class II medical device recall Z-0738-2017

Terminated recall by C.R. Bard, Inc., reported 2016-12-21, distributed nationwide. Package Defect: Products may be at risk for having a slit defect on the package and that may affect the produc

Recall number	`Z-0738-2017`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	C.R. Bard, Inc., Covington, GA, United States
Recall initiated	2016-08-03
Classified	2016-12-12
Reported by FDA	2016-12-21
Terminated	2021-10-05
Distributed	Nationwide (US)
Countries outside the US	AU, CA, FR, IT, MX, NZ
Reason classes	sterility, packaging
Lot numbers	`NGZC4950`, `NGZD2121`, `NGZD4043`, `NGZD4876`, `NGZE2323`, `NGZE3389`, `NGZF0189`, `NGZF2494`, `NGZF4014`

Product

BARDIA¿ 60cc Piston Irrigation Syringe, Sterile, Rx Only, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer adapter tip are included. BARD¿ Syringe allows one-hand use with a 60cc or 70cc graduated barrel and thumb-ring plunger and is indicated for catheter irrigation use. BARD¿ Syringe is intended for Cytoscope or Resectoscope irrigation, catheter irrigation and Foley catheter balloon inflation.

Reason for recall

Package Defect: Products may be at risk for having a slit defect on the package and that may affect the product sterility.

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-0738-2017. 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.