# FDA recall Z-0487-2024

> **Remington Medical, Inc.** · Class II · device recall initiated 2023-11-03.

## Product

Remington MEDICAL Drainage Bag, REF 600-D;

## Reason for recall

There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.

## Distribution

US:  PA and FL

## Key facts

- **Recall number:** Z-0487-2024
- **Recalling firm:** Remington Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-03
- **Report date:** 2023-12-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Alpharetta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0487-2024

## Citation

> AI Analytics. FDA recall Z-0487-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0487-2024. Source: US FDA. Licensed CC0.

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