# FDA recall Z-1308-2018

> **C.R. Bard, Inc.** · Class II · device recall initiated 2017-09-14.

## Product

Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box, each catheter is packaged in an individual pouch.  Urinary catheter.

## Reason for recall

Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.

## Distribution

US Nationwide in the states of AK, AL, AR, AZ, CA, FL, GA, HI, IA, ID, KS, KY, MD, ME, MI, MN, MO, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, including Puerto Rico

## Key facts

- **Recall number:** Z-1308-2018
- **Recalling firm:** C.R. Bard, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-14
- **Report date:** 2018-04-11
- **Termination date:** 2019-11-05

- **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-1308-2018

## Citation

> AI Analytics. FDA recall Z-1308-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1308-2018. Source: US FDA. Licensed CC0.

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