# FDA recall Z-1205-2018

> **Johnson & Johnson Consumer, Inc.** · Class II · device recall initiated 2017-12-18.

## Product

Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 1in)

## Reason for recall

Johnson & Johnson Consumer Inc. is initiating a voluntary, Class II recall at the retail level in the U.S. of select COACH¿ Self-Adhering Sports Wraps, BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wraps and BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wraps products. The current labeling claim states  not made with natural rubber latex  which needs to be updated based upon recent awareness that natural latex was used as a base ingredient in the early-stage manufacturing process, which reduces the allergic protein found in natural latex.

## Distribution

Nationally

## Key facts

- **Recall number:** Z-1205-2018
- **Recalling firm:** Johnson & Johnson Consumer, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-18
- **Report date:** 2018-04-04
- **Termination date:** 2020-04-14

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1205-2018

## Citation

> AI Analytics. FDA recall Z-1205-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1205-2018. Source: US FDA. Licensed CC0.

---

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