PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: September 5, 2018 Initiated: February 1, 2018 #Z-2948-2018

Product Description

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.

Details

Recalling Firm
Medline Industries Inc
Units Affected
90,870 units
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
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing only.. Recalled by Medline Industries Inc. Units affected: 90,870 units.
Why was this product recalled?
Packaged with an incorrect overwrap.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 5, 2018. Severity: Moderate. Recall number: Z-2948-2018.