# FDA recall Z-1630-2018

> **Integra LifeSciences Corp.** · Class II · device recall initiated 2018-03-06.

## Product

Manuka Honey Wound Gel  Catalogue No: 716597    Product Usage:  Helps maintain a moist wound environment which has shown to be conducive to wound healing Ideal for minor scalds and burns, minor cuts, lacerations and minor abrasions

## Reason for recall

Incorrect gel part number listed in a master manufacturing record

## Distribution

US state of RI

## Key facts

- **Recall number:** Z-1630-2018
- **Recalling firm:** Integra LifeSciences Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-06
- **Report date:** 2018-05-16
- **Termination date:** 2018-07-30

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1630-2018

## Citation

> AI Analytics. FDA recall Z-1630-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1630-2018. Source: US FDA. Licensed CC0.

---

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