Devices

Device Recall CADD Administration Set, 21733924, Rx Only, Sterile EO.

Model / Serial
46X817, 46X829, 46X899, 46X828, 46X896, 46X990, 46X831, 46X897, 46X1001.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
US:AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WV, WY. OUS: Canada
Product Description
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Manufacturer
Smiths Medical ASD Inc.
1 Event
- Recall of Device Recall CADD Administration Set, 21733924, Rx Only, Sterile EO.

Manufacturer

Smiths Medical ASD Inc.

Manufacturer Address
Smiths Medical ASD Inc., 6000 Nathan Ln N, Minneapolis MN 55442-1690
Manufacturer Parent Company (2017)
Smiths Group Plc
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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