# FDA recall Z-1273-2022

> **Bard Peripheral Vascular Inc** · Class II · device recall initiated 2022-04-22.

## Product

REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,

## Reason for recall

There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr needle instead of a 6 Fr needle. They can be used in conjunction with the following drainage methods:  Universal extension set and drainage bag, vacuum bottle, and wall suction.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of MS, NC, FL, KS, GA, OH, AZ, NV, OH, IL, MI, MO,IA, CA, PA, AL,WA, TN, IN, NY and the countries of AU, BE, NZ.

## Key facts

- **Recall number:** Z-1273-2022
- **Recalling firm:** Bard Peripheral Vascular Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-22
- **Report date:** 2022-06-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1273-2022

## Citation

> AI Analytics. FDA recall Z-1273-2022. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1273-2022. Source: US FDA. Licensed CC0.

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