# FDA recall Z-2984-2026

> **Bard Access Systems, Inc.** · Class I · device recall initiated 2026-08-10.

## Product

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150;   Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200;   Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605240;  Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605300;  Power-Trialysis Short-Term Curved Extension Dialysis Catheter, REF: 5615120;  Power-Trialysis Short-Term Curved Extension Dialysis Catheter, REF: 5615150;  Power-Trialysis Short-Term Curved Extension Dialysis Catheter, REF: 5615200;   Power-Trialysis Short-Term Curved Extension Dialysis Catheter, REF: 5615240;  Power-Trialysis Short-Term Alphacurve Dialysis Catheter, REF: 5655120;   Power-Trialysis Short-Term Alphacurve Dialysis Catheter, REF: 5655150;   Power-Trialysis Short-Term Alphacurve Dialysis Catheter, REF: 5655200;  Power-Trialysis Short-Term Alphacurve Dialysis Catheter, REF: 5655240;   Power-Trialysis Short-Term Straight Dialysis Catheter Full Procedure Tray, REF: 5605200G;   Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter, REF: 5855200G;   Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter, REF: 5865150G;    Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter, REF: 5855150;  Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter, REF: 5855200;  Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter, REF: 5855240;  Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter, REF: 5855300;  Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter, REF: 5865120;  Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter, REF: 5865150;  Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter, REF: 5865200;  Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter, REF: 5865240

## Reason for recall

this is a downstream recall of class I recall RES 98777

## Distribution

US: FL, IL, OH, VA, MD, TX, WI, GA, TN, IN, SC, NC, MI, PA, OR, OK, AZ, MS, NJ, AL, CA, CO, MA, NV, ID, MO, LA, WA, KY, IA, NH, NY, KS, HI, NE, MN, MT, WY, AR, RI, WV, UT, PR, DE, CT, ME, DC, ND, NM, SD

## Key facts

- **Recall number:** Z-2984-2026
- **Recalling firm:** Bard Access Systems, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-08-10
- **Report date:** 2026-09-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salt Lake City, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2984-2026

## Citation

> MORVS. FDA recall Z-2984-2026. Retrieved 2026-10-14 from https://api.morvs.ai/recall/Z-2984-2026. Source: US FDA. Licensed CC0.

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