# FDA recall Z-1089-2022

> **Total Resources Intl** · Class II · device recall initiated 2022-03-11.

## Product

Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113, 10HBC01329GLRV1, 10OUT02086GLRV2, 16BLU01495, 20HBC01015CCREV3, 20HBC01084GLOWCC.  Kit contents include ULTRAtab Laboratories Coated APAP 325 mg (Acetaminophen 325 mg), Product Code: L202L.

## Reason for recall

ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due to a Fluid Bed Drier exhaust system breach, which presents the possibility of cross-contamination where the potential contaminations are well known API's at well below efficacious dose levels.

## Distribution

US: IL, PA, VA, AR, TX, IA, DE, GA, NY, LA, AL, IN, MI, MO, NC, KS, CO, AZ, OH, MS, CA, FL, WI, KY, UT, OR, NH, TN, NV, CT

## Key facts

- **Recall number:** Z-1089-2022
- **Recalling firm:** Total Resources Intl
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-03-11
- **Report date:** 2022-05-25
- **Termination date:** 2025-01-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** City of Industry, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1089-2022

## Citation

> AI Analytics. FDA recall Z-1089-2022. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-1089-2022. Source: US FDA. Licensed CC0.

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