# FDA recall Z-2948-2018

> **Medline Industries Inc** · Class II · device recall initiated 2018-02-01.

## Product

Medline 0.9 % Sodium Chloride Injection, USP   5 mL in 10 mL Syringe ZR       Intended for flushing IV catheters and IV tubing only.

## Reason for recall

Packaged with an incorrect overwrap.

## Distribution

US Nationwide Distribution to states of: CA, CT, DE, FL, GA, IN, LA, MA, MD, MN, MS, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, VA, VT, WA and WV

## Key facts

- **Recall number:** Z-2948-2018
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-02-01
- **Report date:** 2018-09-05
- **Termination date:** 2020-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2948-2018

## Citation

> AI Analytics. FDA recall Z-2948-2018. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2948-2018. Source: US FDA. Licensed CC0.

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