• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 1 Device Recall Nimbus II Ambulatory Infusion Pump

  • 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 Nimbus II Ambulatory Infusion Pump see related information
Date Initiated by Firm February 21, 2024
Date Posted March 28, 2024
Recall Status1 Open3, Classified
Recall Number Z-1286-2024
Recall Event ID 94124
510(K)Number K140783  K153193  
Product Classification Pump, infusion - Product Code FRN
Product Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components
Code Information UDI-DI: Nimbus II PainPRO: UDI-DI 00817170020086, Lots AHZ081-190619096 AHZ081-200229480 AHZ081-2004171062 AHZ081-200517528 AHZ081-200714696 AHZ081-2009231440 AHZ081-201105480 AHZ081-201105360 AHZ081-201208288 AHZ081-2012081944 AHZ081-2012081944 AHZ081-2108141920 AHZ081-211123360 AHZ081-2111242568 AHZ081-22062072 A100G-170420044 A100G-170512429 AGZ049-170512429 AGZ049-170615116 AGZ049-170816391 AGZ049-170829480 AGZ049-1709071188 AGZ049-171027828 AGZ049-1712011824 AGZ049-171229744 AGZ049-1806091272 AGZ049-180626984 AGZ049-1809201152 AGZ049-1810241536 AGZ049-181102108 AGZ049-190104504 AGZ049-190104648 AGZ049-190314768 AGZ049-1903151440 AGZ049-190515480 AGZ049-190515960 AGZ049-1906271440 AGZ049-1907231776 AGZ049-190723360 AGZ049-190806144 AGZ049-190924504 AGZ049-191023480 AGZ049-1912161920 AGZ049-200102576 AGZ049-2002251632 AGZ049-200714960 AGZ049-200828960 AGZ049-2009241440 AGZ049-2011301920 AGZ049-2103231200 AGZ049-210324360 AGZ049-210422528 AGZ049-210809480 AGZ049-211121360 AGZ049-2111222136 AGZ049-2202064320 AGZ049-220207720 AGZ049-220629624 AGZ049-2208091920 AGZ049-2312141632 AGZ049-2312271440 AGZ049-2401081344; Nimbus II Flex: UDI-DI 00817170020093 Lots AGZ050-170621081 AGZ050-170622027 AGZ050-170623297 AGZ050-170829240 AGZ050-171027180 AGZ050-180402360 AGZ050-180517720 AGZ050-190527480 AGZ050-190813360 AGZ050-190910360 AGZ050-190924720 AGZ050-200114300 AGZ050-210219600; Nimbus II Plus: UDI-DI 00817170020161 Lots AJZ074-190215120 AJZ074-190513120 AJZ074-190722360 AJZ074-20010379 AJZ074-200417282 AJZ074-200604960 AJZ074-200903960 AJZ074-210219720 AJZ074-210303180 AJZ074-210325960 AJZ074-2111081200 AJZ074-2202072880 AJZ074-2206012640 AJZ074-2206213120 AJZ074-2208092040 AJZ074-2208092640; Nimbus II EpiD: UDI-DI 00817170020376 Lot ALZ103-200824420; Nimbus II EMS: UDI-DI 00817170020109 Lots AGZ057-170925120 AGZ057-171027300; HS-001 Nimbus Administration Set: 00817170020017 HS-002 Nimbus Administration Set: 00817170020048 HS-003 Nimbus Administration Set: 00817170020024 HS-004 Nimbus Administration Set: 00817170020031 HS-008 Nimbus Administration Set: 00817170020123 All units are recalled.
Recalling Firm/
Manufacturer
InfuTronix LLC
177 Pine St
Natick MA 01760-1331
For Additional Information Contact Customer Service
508-650-2008
Manufacturer Reason
for Recall
InfuTronix is removing the Nimbus Infusion Pump Systems from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product leakage, high or low flow rate, or damaged pump housing. The device will not be available or supported after June 20, 2024.
FDA Determined
Cause 2
Device Design
Action On February 21, 2024, the firm began notifying customers via URGENT MEDICAL DEVICE REMOVAL letters. Customers were informed that the identified Nimbus Infusion Pumps are being removed from the market. The products will no longer be supported by InfuTronix for the Nimbus Infusion Pumps or related infusion sets beyond June 20, 2024. Customers of InfuTronix who have Nimbus Infusion Pumps and associated infusion sets in their possession should contact InfuTronix customer service at Customerservice@intuvie.com, where they will be instructed on the Return Material Authorization (RMA) process to be followed for returning the both the Nimbus Infusion Pumps and associated infusion sets. As the device will not be available or supported after June 20, 2024, InfuTronix encourages the healthcare provider to seek alternative methods of drug product infusion appropriate for their patient s needs, based on their medical expertise, at the earliest possible opportunity. ***Updated 4/12/24*** The firm issued updated letters on 4/9/24 to reflect that the recall had been classified Class I by the FDA. Effective immediately, Nimbus Pumps will no longer be shipped. However, administration sets will continue to be shipped through June 20, 2024.
Quantity in Commerce 52,328 total
Distribution Domestic US distribution nationwide. No international distribution.
Total Product Life Cycle TPLC 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) Database 510(K)s with Product Code = FRN and Original Applicant = ZYNO MEDICAL LLC
510(K)s with Product Code = FRN and Original Applicant = ZYNO MEDICAL LLC.
-
-