# FDA recall Z-2229-2021

> **Shent USA, Inc.** · Class II · device recall initiated 2021-01-12.

## Product

Grasper/Retriever, Alligator Jaw 2.4 mm x 5 mm x 230 cm Catalog Number: 7208     Intended use: single use accessory devices used through the working channel of a GI endoscope

## Reason for recall

Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator Jaw, 2.4 mm x 5 mm x 230 cm) may actually be catalog #7226 (Grasper/Retriever, Alligator Jaw, 2.4 mm x 5 mm x 8 mm x 230 cm) and  Devices labeled as catalog #7226,  (Grasper/Retriever, Alligator Jaw, Rat Tooth, 2.4 mm x 8 mm x 230 cm) may actually be catalog #7208, Grasper/Retriever, Alligator Jaw, 2.4 mm x 5 mm x 230  cm).

## Distribution

US Nationwide Distribution - CA, CO, MI  Foreign: Australia

## Key facts

- **Recall number:** Z-2229-2021
- **Recalling firm:** Shent USA, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2021-01-12
- **Report date:** 2021-08-18

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2229-2021

## Citation

> AI Analytics. FDA recall Z-2229-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2229-2021. Source: US FDA. Licensed CC0.

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