# FDA recall Z-2075-2025

> **C.R. Bard Inc** · Class II · device recall initiated 2025-06-03.

## Product

BD Heyman Follower Coude Tip  for following sizes:    12Fr - REF:021312  14Fr - REF:021314,  16Fr - REF: 021316

## Reason for recall

Cather packaging may contain the incorrect French size.

## Distribution

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, FL, GA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WI, WV and the country of Canada.

## Key facts

- **Recall number:** Z-2075-2025
- **Recalling firm:** C.R. Bard Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-03
- **Report date:** 2025-07-09

- **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-2075-2025

## Citation

> AI Analytics. FDA recall Z-2075-2025. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-2075-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*