BD Posiflush Pre-Filled Normal Saline Syringes (2019-10-07)

Starting date:

October 7, 2019

Posting date:

November 1, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-71455

Last updated: 2019-11-01

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  Reason
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  Affected products

Affected Products

BD Posiflush Pre-Filled Normal Saline Syringes

Reason

Product in the shelf carton was mixed, customer found product with barrel label stating '""POSIFLUSH EXPERIMENTAL PRODUCT, For Investigational Use Only/Not for Human Use"".

Affected products