PlainRecalls
FDA Devices Moderate Class II Terminated

Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide.

Reported: August 2, 2017 Initiated: December 9, 2016 #Z-2759-2017

Product Description

Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide.

Reason for Recall

The label of the CADD Blue-Striped Administrative Set is missing the expiration date, which is considered a regulatory compliance issue for Canada.

Details

Recalling Firm
Smiths Medical ASD Inc.
Units Affected
641,070 units
Distribution
Canada only
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide.. Recalled by Smiths Medical ASD Inc.. Units affected: 641,070 units.
Why was this product recalled?
The label of the CADD Blue-Striped Administrative Set is missing the expiration date, which is considered a regulatory compliance issue for Canada.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 2, 2017. Severity: Moderate. Recall number: Z-2759-2017.