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Advocates, State Health Officials: Naloxone In Indiana Likely Not Part Of Recall

By Indiana Public Media News Staff

Posted June 6, 2018

State health officials and a nonprofit organization both say none of the naloxone they distribute is included in a recent voluntary recall.

Naloxone manufacturer Hospira issued a voluntary recall of its single-use cartridge syringe system for the opioid overdose antidote.

The company says it found loose or embedded particulate matter on the syringe plunger.

The recall is on lot numbers 72680LL and 76510LL.

If someone is exposed to the particulate, Hospira says there is a low chance of experiencing adverse health effects, including allergic reactions and pulmonary dysfunction. The company says it has not received any complaints about the items affected by the recall.

A representative from the Indiana State Department of Health said none of the naloxone distributed by the department is part of the recall.

The nonprofit Overdose Lifeline distributes naloxone units to health departments, organizations and individuals across the state.

In a statement, the group says community distribution entities in Indiana don't use the type of naloxone system that's been recalled.

This story has been updated.

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