FDA recall Z-2544-2021

B. Braun Medical, Inc. · Class II · device

Product

15 drops/ml, Priming Volume: 27ml, Length: 129 in. Single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluid Material ID: 354212

Reason for recall

Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration of medications, under-delivery or incomplete dosing and bloodstream infections.

Distribution

Worldwide distribution - US Nationwide distribution and the country of Canada.

Key facts

Status
Terminated
Initiation date
2021-08-10
Report date
2021-10-06
Termination date
2024-09-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Allentown, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2544-2021