# FDA recall Z-3114-2026

> **C.R. Bard Inc** · Class II · device recall initiated 2026-06-25.

## Product

Products that contain the Pericare Wipes:    Bardex Lubricath Foley Catheter Tray  REF:  899914  899916  899918  UDI codes:  00801741024801¿	10801741024808  00801741024818¿	10801741024815  00801741024825¿	10801741024822    SureStep" Foley Tray System with Bardex¿ Lubricath Temp Sensing Foley Catheter  REF: A119416M  UDI code: 00801741073700	10801741073707  	  SureStep" Foley Tray System Bard¿ Lubricath Foley  REF: A800361  UDI code: 00801741073939	10801741073936  	  SureStep" Foley Tray System Bard¿ Lubricath¿ Foley Catheter Tray  REF: A899616  UDI code: 00801741104534¿	10801741104531    SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter  REF: A899914  UDI code: 00801741074004	10801741074001    SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter  REF: A899916  UDI code: 00801741074011¿	10801741074018    SureStep" Foley Tray System Bardex¿ Lubricath¿ Temperature Sensing Catheter  REF: A900216  UDI code: 00801741120978¿	10801741120975    SureStep" Foley Tray System Bard¿Lubricath¿ Foley Catheter  REF:  A902914  A902916  A902918  UDI code:  00801741074066¿10801741074063  00801741074073	10801741074070  00801741074080¿10801741074087    Bard¿ Urine Meter Foley Catheter Tray With Bardex¿ Lubricath¿ Foley Catheter  REF: 304916  UDI code: 00801741019736	01801741019739    Bard¿ Urine Meter Foley Catheter Tray With Bardex¿ Lubricath¿ Foley Catheter  REF: 902916  UDI codes: 00801741024863	10801741024860    (416A) SureStep Foley Tray System Bardex IC Complete Care (714A/716A/718A)SureStep Foley Tray System Bardex IC Complete  REF:  A304914  A304916  A304918  UDI codes:   00801741104350¿	10801741104357  00801741104367¿	10801741104364  00801741100499¿	10801741100496    SureStep" Foley Tray System Bard¿ Lubricath Foley  REF: A800365  UDI codes: 00801741073960	10801741073967    SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter  REF: A899918  UDI codes: 00801741074028	10801741074025    SureStep" Foley Tray System Bard¿Lubricath¿ Foley Catheter  REF: A902618  UDI codes: 00801741104640	10801741104647    SureStep" Foley Tray System Bard¿Lubricath¿ Foley Catheter  REF: A902616  UDI codes: 00801741104633¿	10801741104630    SureStep Intermittent Catheter Tray  REF: INTL16C  UDI codes: 00801741183195¿	10801741183192  	  	  	  	  	        For urological use only, Intended for use in the drainage and/or collection and/or measurement of urine.

## Reason for recall

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

## Distribution

Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Costs Rica, Guatemala, Mexico, Saudi Arabia, and United Arab Emirates.

## Key facts

- **Recall number:** Z-3114-2026
- **Recalling firm:** C.R. Bard Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-25
- **Report date:** 2026-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Covington, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3114-2026

## Citation

> MORVS. FDA recall Z-3114-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-3114-2026. Source: US FDA. Licensed CC0.

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