13

Apr

2007

Inc., Class II Smiths Medical MD

infusionpump, recall

0

Company:Smiths Medical MD, Inc., .
Date of Enforcement Report:4/11/2007
Class:ll

PRODUCT
Deltec branded CADD-Prizm PCS II ambulatory infusion pump and the CADD-Prizm VIP system ambulatory infusion pumps; (Both) Model 6101; Order #21-8861-01 (PCS II) and 21-8821-01 (VIP); RX ONLY, Recall # Z-0718-2007

REASON
The year of manufacture had been incorrectly entered as 1980 into the pumps software during the manufacture process. As a result the pump may go into an immediate ‘Clock battery is Low/Service Immediately’ or ‘Clock Battery needs service soon’ alarm message indicating that the pump requires servicing.

CODE
Serial numbers affected: 691099, 691108, 691117, 691700, 691704, 691713, 691719, 691724, 691729, 691731, 691734, 691737, 691739, 691744, 691748, 691756, 691761, 691764, 691769, 691772, 691776, 691780, 691785, 691788, 691793, 691794, 691798.

RECALLING FIRM/MANUFACTURER
Smiths Medical MD, Inc., Saint Paul, MN, by telephone on February 1, 2007. Firm initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE
27 units

DISTRIBUTION
Nationwide

About the author

Amy Sellers

Amy enjoys researching and writing about developments in medical technology and how that intersects with US law. She received her J.D. from the University of Florida Levin College of Law in 2020 and now works as a Regulatory Associate for SoftwareCPR®, a general-purpose regulatory consulting firm that is recognized globally for their expertise with standards and national regulations pertaining to medical device, mobile medical app, and HealthIT software.

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