# FDA recall Z-1170-2021

> **Boston Scientific Corporation** · Class II · device recall initiated 2021-01-19.

## Product

Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares    Outer box UPN, Inner pouch UPN:    M00560311 (Box 5), M00560310;    M00560321 (Box 5), M00560320;   M00562651 (Box 5), M00562650;    M00562652 (Box 20), M00562650;    M00562671 (Box 5), M00562670;    M00562672 (Box 20), M00562670;    M00562673 (Box 40), M00562670;    M00562691 (Box 5); M00562690;    M00562692 (Box 20), M00562690;    M00562693 (Box 40), M00562690.

## Reason for recall

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

## Distribution

US nationwide distribution.

## Key facts

- **Recall number:** Z-1170-2021
- **Recalling firm:** Boston Scientific Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-01-19
- **Report date:** 2021-03-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marlborough, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1170-2021

## Citation

> AI Analytics. FDA recall Z-1170-2021. Retrieved 2026-09-22 from https://api.ai-analytics.org/recall/Z-1170-2021. Source: US FDA. Licensed CC0.

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