# FDA recall Z-1701-2021

> **Zavation** · Class II · device recall initiated 2021-03-25.

## Product

10 GAUGE CEMENT DELIVERY CANNULA, INTVM-CDC.  For use in Orthopedic / spinal procedures.

## Reason for recall

Products distributed as sterile may not have been adequately sterilized

## Distribution

US nationwide distribution.

## Key facts

- **Recall number:** Z-1701-2021
- **Recalling firm:** Zavation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-03-25
- **Report date:** 2021-06-09
- **Termination date:** 2023-03-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Flowood, MS, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1701-2021

## Citation

> AI Analytics. FDA recall Z-1701-2021. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1701-2021. Source: US FDA. Licensed CC0.

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