Opticap Disconnect Cap with Povidone-Iodine Solution (2021-03-10)

Starting date:

March 10, 2021

Posting date:

March 25, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-75203

Last updated:
2021-03-25

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  Reason
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  Affected products

Affected Products 

Opticap Disconnect Cap with Povidone-Iodine Solution

Reason

Baxter Corporation is issuing a voluntary medical device recall for a single lot of Opticap Disconnect Caps that was distributed by Baxter between February 17, 2021 and February 23, 2021. Baxter is taking this action as a precautionary measure as this product is past its labelled expiry and was inadvertently shipped to customers.  This recall only pertains to customers who received the product after its expiration.

Affected products