# FDA recall Z-1475-2024

> **3M Company - Health Care Business** · Class II · device recall initiated 2024-02-20.

## Product

3M Tube Securement Device, Small, 1.7 IN/PO x 2.4 IN/PO, REF 1500U, Sterile; and 3M Tube Securement Device, Large, 2.2 IN/PO x 3.5 IN/PO, REF 1501U, Sterile.  Product is packaged 1 device per pouch, 25 pouches per primary carton, and 4 primary cartons per shipper box.

## Reason for recall

Manufacturing nonconformities are in some lots of the Tube Securement Device, such as the top film layer may be partially or completely missing and some devices may exhibit the appearance of an incorrect shape due to excess material not being removed from the product liner.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of CA, CO, FL, IA, IL, IN, KS, MD, MN, NC, NH, NY, OH, PA, TX, VA, and WA, including PR. The countries of Australia, Austria, Canada, China, Finland, Germany, Ireland, New Zealand, Norway, Poland, Sweden, and the United Kingdom.

## Key facts

- **Recall number:** Z-1475-2024
- **Recalling firm:** 3M Company - Health Care Business
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-20
- **Report date:** 2024-04-10

- **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-1475-2024

## Citation

> AI Analytics. FDA recall Z-1475-2024. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1475-2024. Source: US FDA. Licensed CC0.

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