Medical device recalls Moderate risk

Medline Industries Inc recalls Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing…

Recall date
February 1, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2948-2018
FDA classification
Class II
Brand / firm
Medline Industries Inc
Sold / distributed
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

Why it was recalled

Packaged with an incorrect overwrap.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What 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.

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