# FDA recall Z-1809-2022

> **Mckesson Medical-Surgical Inc. Corporate Office** · Class III · device recall initiated 2022-05-25.

## Product

a.  DYNAREX Nice'n Fresh WIPE, BABY WET 6X6.75" (140/CN12CN/CS) Catalog # 1313.    b.  DYNAREX DynaCare WIPE, WET FLUSHABLE ADULT 9X13" (24/PK 24PK/CS) Catalog # 1322.      c.  DYNAREX dynacare WIPE, WET FLUSHABLE JR 5X8" (42/BX 12BX/CS) Catalog # 1324

## Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1809-2022
- **Recalling firm:** Mckesson Medical-Surgical Inc. Corporate Office
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-25
- **Report date:** 2022-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Richmond, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1809-2022

## Citation

> AI Analytics. FDA recall Z-1809-2022. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1809-2022. Source: US FDA. Licensed CC0.

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