# FDA recall Z-1165-2026

> **Cerapedics, Inc.** · Class II · device recall initiated 2025-12-29.

## Product

PearMatrix P-15 Peptide Enhanced Bone Graft  Bone Graft, 1.0cc  REF: 730-010

## Reason for recall

Incorrect expiration date

## Distribution

US Nationwide distribution in the states of CA, CO, CT, FL, GA, ID, IL, KS, LA, MI, MN, MO, MT, NE, NJ, NV,  NY, OH,OR, PA, TN, TX, WA, WY.

## Key facts

- **Recall number:** Z-1165-2026
- **Recalling firm:** Cerapedics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-29
- **Report date:** 2026-02-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Westminster, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1165-2026

## Citation

> AI Analytics. FDA recall Z-1165-2026. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1165-2026. Source: US FDA. Licensed CC0.

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