# FDA recall Z-1623-2022

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

## Product

a. DERMA SCIENCES, INC.	NG Strip	FASTENER, NASAL TUBE IND WRAP(25/BX), Catalog NG25.      b.  DERMA SCIENCES, INC. Surgitube BANDAGE, GAUZE #2P 7/8"X50YDS DERSCI Catalog GL-242.    c.  DERMA SCIENCES, INC. Surgilast TUBE NET SZ3 MED 10YDS/EA HAND, ARM, LEG, FOOT SURGILAST Catalog # GL103.    d.  DERMA SCIENCES, INC. Surgitube & Surgigrip APPLICATOR, SURGITUBE/GRIP METAL SZ3 6" CHLD/ADLT DERSCI Catalog #GL-234.

## 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

## Key facts

- **Recall number:** Z-1623-2022
- **Recalling firm:** Mckesson Medical-Surgical Inc. Corporate Office
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-25
- **Report date:** 2022-08-31

- **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-1623-2022

## Citation

> AI Analytics. FDA recall Z-1623-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1623-2022. Source: US FDA. Licensed CC0.

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