Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 1 Device Recall CADDSolis VIP

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 1 Device Recall CADDSolis VIPsee related information
Date Initiated by FirmApril 10, 2025
Date PostedMay 07, 2025
Recall Status1 Open3, Classified
Recall NumberZ-1668-2025
Recall Event ID 96620
510(K)NumberK111275 
Product Classification Pump, infusion - Product Code FRN
ProductCADD-Solis VIP Ambulatory Infusion Pump; Model/Number: 21-2120-0100-02 21-2120-0100-03 21-2120-0100-06 21-2120-0100-232 21-2120-0100-233 21-2120-0100-50 21-2120-0100-51 21-2120-0100-95 21-2120-0102-02 21-2120-0102-03 21-2120-0102-06 21-2120-0102-07 21-2120-0102-08 21-2120-0102-12 21-2120-0102-13 21-2120-0102-14 21-2120-0102-15 21-2120-0102-17 21-2120-0102-237 21-2120-0102-238 21-2120-0102-247 21-2120-0102-249 21-2120-0102-51 21-2120-0102-78 21-2120-0102-92 21-2120-0102-97 21-2120-0102-98 21-2120-0103-01 21-2120-0103-02 21-2120-0103-03 21-2120-0103-06 21-2120-0103-07 21-2120-0103-08 21-2120-0103-12 21-2120-0103-14 21-2120-0103-15 21-2120-0103-17 21-2120-0103-249 21-2120-0103-51 21-2120-0103-78 21-2120-0104-01 21-2120-0104-231 21-2120-0105-00 21-2120-0105-01 21-2120-0105-02L 21-2120-0105-03L 21-2120-0105-06L 21-2120-0105-07L 21-2120-0105-08 21-2120-0105-08L 21-2120-0105-12L 21-2120-0105-13L 21-2120-0105-14L 21-2120-0105-15L 21-2120-0105-17L 21-2120-0105-50 21-2120-0105-50L 21-2125-0104-01 21-2125-0105-03L 21-2125-0105-07L 21-2125-0105-08L 21-2125-0105-50L 21-2127-0104-01 21-2127-0105-01 21-2127-0105-02L 21-2127-0105-03L 21-2127-0105-06L 21-2127-0105-08L 21-2127-0105-50L
Code Information All CADD-Solis and CADD-Solis VIP Ambulatory Infusion Pumps UDI-DI: 10610586034787 10610586038778 10610586038785 10610586038808 10610586038822 10610586039232 10610586041037 10610586041051 10610586042591 10610586042669 10610586042829 10610586042836 15019517084368 15019517096378 15019517096385 15019517096392 15019517099690 15019517101003 15019517101010 15019517101034 15019517101041 15019517126587 15019517126594 15019517126600 15019517126617 15019517128697 15019517135343 15019517149999 15019517150001 15019517150292 15019517154290 15019517154887 15019517154924 15019517154979 15019517154986 15019517154993 15019517155006 15019517155013 15019517155044 15019517246735 15019517247008 15019517247169 15019517247176 15019517247183 15019517247206 00610586038900 00610586039310 04546027095620 04546027095637 04546027095644 04546027095668 04546027095675 04546027095682 04546027095699 04546027095705 04546027095712 04546027095729 04546027095736 04546027095743 04546027095897 04546027095903 04546027095910 04546027422983 04546027424116 04546027424130 04546027424147 04546027424178 04546027424185 04546027424192 04546027424208 04546027424598 05019517154934 05019517155108 10610586031854 10610586033933 10610586033940 10610586035067 10610586035357 10610586035395 10610586035401 10610586035418 10610586035432 10610586035456 10610586035494 10610586038501 10610586038518 10610586038792 10610586038839 10610586038860 10610586038891 10610586038914 10610586038921 10610586038938 10610586038952 10610586038969 10610586038983 10610586038990 10610586039010 10610586039041 10610586039065 10610586039072 10610586039089 10610586039195 10610586039256 10610586039270 10610586039409 10610586039416 10610586039430 10610586039447 10610586039454 10610586039461 10610586039478 10610586039485 10610586039492 10610586040429 10610586040443 10610586040528 10610586041822 10610586042607 10610586042614 10610586042843 15019517084382 15019517084399 15019517084405 15019517084412 15019517084429 15019517084443 15019517084450 15019517084467 15019517086720 15019517149517 15019517149975 15019517150025 15019517150032 15019517150049 15019517150056 15019517150063 15019517150070 15019517150087 15019517150094 15019517150100 15019517150117 15019517150124¿ 15019517150131 15019517150179 15019517150193 15019517150216 15019517150278 15019517150308 15019517150315 15019517150322 15019517150391 30610586035344 30610586035368 30610586035511 30610586039205 30610586039397 30610586040430 30610586040539 35019517128677 35019517128684 35019517128691 35019517128721 35019517128738 35019517128745 35019517128769 35019517128783 35019517128837 35019517135316 35019517135323 35019517135330 35019517135354 35019517135361 35019517154850 35019517154867 35019517154874 35019517154904 35019517154911 35019517154942 35019517154959 35019517154966 35019517155031 35019517155055 35019517155062 35019517155079 35019517155086 35019517155130
Recalling Firm/
Manufacturer		 Smiths Medical ASD, Inc.
6000 Nathan Ln N
Minneapolis MN 55442-1690
For Additional Information ContactTechnical Support
800-241-4002
Manufacturer Reason
for Recall		Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
FDA Determined
Cause 2		Labeling design
ActionOn April 10, 2025, the firm notified affected consignees via letters titled "Urgent Medical Device Correction." Customers were informed of conditions under which the false Upstream Occlusion Alarm may occur. The USO alarm can be cleared during these conditions by removing the administration from the pump, re-attaching the administration set, and restarting delivery. Customers should verify there is no upstream occlusion present. The firm will be making an update to the Infusion Pump Operator's Manual to include these conditions.
Quantity in Commerce185,975 US; 127,701 OUS Total
DistributionWorldwide - US nationwide distribution.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = FRN
-
-