# FDA recall Z-1056-2022

> **Cerapedics, Inc.** · Class III · device recall initiated 2022-04-14.

## Product

putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY

## Reason for recall

Patient chart label contains incorrect Part Number and volume amount.

## Distribution

U.S. Nationwide distribution in the states of  AL, AZ, CA, CT, DC, DE, ID, IN, KS, KY, MD, MI, MN, MO, NC, NV, NY, OH, PA, TX, VA, and WA.

## Key facts

- **Recall number:** Z-1056-2022
- **Recalling firm:** Cerapedics, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-04-14
- **Report date:** 2022-05-18
- **Termination date:** 2024-12-23

- **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-1056-2022

## Citation

> AI Analytics. FDA recall Z-1056-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1056-2022. Source: US FDA. Licensed CC0.

---

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