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Recall Observatory FDA recall evidence

Device product

Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump System Model/Catalog Number: 8713030U Product Description: Perfusor Space Infusion Pump System, Infusion Pump, 1 each Component: N/A

Z-2433-2024

June 14, 2024

Class II

Product summary

Firm
B Braun Medical Inc
Event
Event 94890
Status
Ongoing
Classification
Class II
Quantity
14949
Official record key
device-enforcement:Z-2433-2024

Official wording

Reason: Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.

Code information: Lot Code: Model No 8713030U; UDI-DI 4046963716745; All Serial Numbers

Distribution pattern: Domestic distribution nationwide. International distribution to Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.