# FDA recall Z-0233-2018

> **Dukal Corp.** · Class II · device recall initiated 2017-06-01.

## Product

BLUE BURN SHEET, STERILE, 60" x 96"; Item 7305, GAM item 30-01    Product Usage - May provide a sterile, barrier environment to protect patient from infection.

## Reason for recall

Intact carton revealed presence of shredded burn sheets

## Distribution

Worldwide distribution - US Nationwide in the states of:  CA, CO, CT, FL, GA, IL, CO, NY, NV, IN, MD, MO, MD OH, TN, TX & WI; and country of  Canada

## Key facts

- **Recall number:** Z-0233-2018
- **Recalling firm:** Dukal Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-01
- **Report date:** 2017-12-20
- **Termination date:** 2018-07-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ronkonkoma, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0233-2018

## Citation

> AI Analytics. FDA recall Z-0233-2018. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-0233-2018. Source: US FDA. Licensed CC0.

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