# FDA recall Z-2688-2024

> **Intrinsic Therapeutics, Inc.** · Class II · device recall initiated 2024-07-25.

## Product

Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A

## Reason for recall

At least two units have been found to be missing a weld.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2688-2024
- **Recalling firm:** Intrinsic Therapeutics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-25
- **Report date:** 2024-08-28

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2688-2024

## Citation

> AI Analytics. FDA recall Z-2688-2024. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-2688-2024. Source: US FDA. Licensed CC0.

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