# FDA recall Z-1226-2023

> **Preat Corp** · Class III · device recall initiated 2023-02-01.

## Product

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.

## Reason for recall

Product is labeled with an incorrect expiration date.

## Distribution

Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, NC, NJ, NY, OK, PA, SC,  SD, TN, TX, UT, VA, WA, WI, and WV.  There was also government distribution. The country of Canada.

## Key facts

- **Recall number:** Z-1226-2023
- **Recalling firm:** Preat Corp
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-01
- **Report date:** 2023-03-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Maria, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1226-2023

## Citation

> AI Analytics. FDA recall Z-1226-2023. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1226-2023. Source: US FDA. Licensed CC0.

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