PlainRecalls
FDA Devices Moderate Class II Terminated

CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.

Reported: March 25, 2015 Initiated: February 2, 2015 #Z-1286-2015

Product Description

CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.

Reason for Recall

Smiths Medical has become aware of an issue with specific lots of 50mL CADD" Medication Cassette Reservoirs (Cassette). Some Cassettes may leak at the sealing area of the pump tube and medication bag. Smiths Medical has received no reports of serious injury or death related to this issue.

Details

Recalling Firm
Smiths Medical ASD, Inc.
Units Affected
48,208 (17,040 US, 31,168 OUS).
Distribution
Worldwide Distribution - US (nationwide) Distribution to the states of : AL, AZ, AR, CA, CO, CT, FL, GA, HI, IL IN, IA, MD, MA, MN, MS, MO, NE, NV, NH ,NJ, NM, NY, NC, OH, OR, PA, SD, TN, TX, UT, VA and WA., and to the countries of : Arab Emirates, Austria, Australia, Belgium, Canada, Switzerland, Colombia, Czech Republic, Germany, Denmark, Spain. Finland, France, United Kingdom (GB) Hungary, Indonesia, Ireland, Italy, Netherlands, Portugal, Sweden, Singapore and South Africa.
Location
Saint Paul, MN

Frequently Asked Questions

What product was recalled?
CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.. Recalled by Smiths Medical ASD, Inc.. Units affected: 48,208 (17,040 US, 31,168 OUS)..
Why was this product recalled?
Smiths Medical has become aware of an issue with specific lots of 50mL CADD" Medication Cassette Reservoirs (Cassette). Some Cassettes may leak at the sealing area of the pump tube and medication bag. Smiths Medical has received no reports of serious injury or death related to this issue.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 25, 2015. Severity: Moderate. Recall number: Z-1286-2015.