# FDA recall Z-2251-2023

> **Microtek Medical Inc.** · Class II · device recall initiated 2023-06-23.

## Product

Equipment and table drapes and Surgical Room Turnover (SRT) Kits:    (1) Ecolab Absorbent Table Cover W/Transfer Sheet & Armboard Covers, Model #ABTSLSAN, 20/case, non-sterile;  (2) Microtek/Ecolab/CleanOp Absorbent Table Cover w/Transfer Sheet, Model ABTSLSN, 25/case, non-sterile;    Surgical Room Turnover (SRT) Kits:    (3) Ecolab Genesys CleanOp Infection Control System, Model ALHS-02, 12/case, non-sterile;  (4) Ecolab Genesys CleanOp Infection Control System, Model ALHS-SS-01, 12/case, non-sterile;  (5) Ecolab CleanOp Infection Control System, Model BPGN-02, 10/case, non-sterile;  (6) Ecolab Genesys CleanOp Infection Control System, Model HFH-02, 12/case, non-sterile;  (7) Ecolab Genesys CleanOp Infection Control System, Model HKHA-02, 15/case, non-sterile;  (8) Ecolab CleanOp Infection Control System, Model JFKSC-01, 15/case, non-sterile;  (9) Ecolab Genesys CleanOp Infection Control System, Model LH-LD-05, 12/case, non-sterile;  (10) Ecolab CleanOp Infection Control System, Model

## Reason for recall

Certain lots of the products have a Naphthalene odor.

## Distribution

Worldwide distribution - US Nationwide and the country of Canada.

## Key facts

- **Recall number:** Z-2251-2023
- **Recalling firm:** Microtek Medical Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-23
- **Report date:** 2023-08-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2251-2023

## Citation

> AI Analytics. FDA recall Z-2251-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2251-2023. Source: US FDA. Licensed CC0.

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