SURESTEP Tray — Class II medical device recall Z-1871-2017
Completed recall by C.R. Bard, Inc., reported 2017-04-26, distributed in CA, CO, FL, GA, IA, IL, IN, KY…. Misbranded: Product labeled, Not made with natural rubber latex, may in fact contain natural rubber latex.
| Recall number | Z-1871-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | C.R. Bard, Inc., Covington, GA, United States |
| Recall initiated | 2017-03-09 |
| Classified | 2017-04-20 |
| Reported by FDA | 2017-04-26 |
| Distributed | CA, CO, FL, GA, IA, IL, IN, KY, LA, MI, MN, MS, NC, NE, NJ, NM, OH, OR, PA, RI, TN, TX, VA, WA |
| Quantity | 5,030 units |
| Reason classes | labeling |
| Lot numbers | NGAV2400 |
Product
SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
Reason for recall
Misbranded: Product labeled, Not made with natural rubber latex, may in fact contain natural rubber latex.
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-1871-2017. 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.