# FDA recall Z-1716-2025

> **Integra LifeSciences Corp. (NeuroSciences)** · Class I · device recall initiated 2025-04-11.

## Product

CODMAN Disposable Perforator, 14mm. Cranial perforator.

## Reason for recall

Inadequate weld that can potentially cause the product to disassemble.

## Distribution

Worldwide distribution - US Nationwide including Puerto Rico and the countries of  Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Dominican Republic, Ecuador, El Salvador, France, French Guiana, Germany, Ghana, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Jordan, Kenya, Korea (the Republic of), Lebanon, Lithuania, Malaysia, Morocco, Nepal, Netherlands, New Zealand, Pakistan, Poland, Portugal, Qatar, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, United Arab Emirates, United Kingdom.

## Key facts

- **Recall number:** Z-1716-2025
- **Recalling firm:** Integra LifeSciences Corp. (NeuroSciences)
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-11
- **Report date:** 2025-05-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Princeton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1716-2025

## Citation

> AI Analytics. FDA recall Z-1716-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1716-2025. Source: US FDA. Licensed CC0.

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