SURESTEP Tray — Class II medical device recall Z-0967-2017
Terminated recall by C.R. Bard, Inc., reported 2017-01-18, distributed in CA, CT, FL, GA, IL, IN, KS, KY…. The product contained a latex catheter instead of a silicone catheter.
| Recall number | Z-0967-2017 |
|---|---|
| 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 | 2016-07-11 |
| Classified | 2017-01-09 |
| Reported by FDA | 2017-01-18 |
| Terminated | 2021-10-05 |
| Distributed | CA, CT, FL, GA, IL, IN, KS, KY, MA, MD, MI, NE, NJ, NM, NV, NY, OR, SC, TN, TX, UT, VA, WA |
| Quantity | 2,690 units |
Product
SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
Reason for recall
The product contained a latex catheter instead of a silicone catheter.
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-0967-2017. 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.