BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension — Class II medical device recall Z-2872-2017
Terminated recall by C.R. Bard, Inc., reported 2017-08-16, distributed nationwide. Customer complaint of a cut in the side of the leg bag, indicating a potential breach of the product's sterile
| Recall number | Z-2872-2017 |
|---|---|
| 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 | 2017-06-02 |
| Classified | 2017-08-10 |
| Reported by FDA | 2017-08-16 |
| Terminated | 2021-07-26 |
| Distributed | Nationwide (US) |
| Quantity | 2,350 units |
| Reason classes | sterility |
| Lot numbers | NGAS4058 |
Product
BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as single unit in thermoformed trays. There are 50 units per case. Product Usage: Vinyl leg bag to be used with male external catheters, Foley catheters, or moth other types of urinary catheters, which are intended for use for bladder management including urine drainage, collection and measurement.
Reason for recall
Customer complaint of a cut in the side of the leg bag, indicating a potential breach of the product's sterile barrier.
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-2872-2017. 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.