Product Safety Recalls

Product Recall Tracker

B Braun Medical Inc Recall 89660

Description: PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions Catalog Number: 8713030U

B Braun Medical Inc Recall 89660 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0819-2022
Event ID89660
Event DescriptionPERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions Catalog Number: 8713030U
Product TypeDevices
DistributionUS Distribution to states of: MA, VT
Quantity6 units
Recall ReasonUnits not properly inspected prior to release to the market, may not function as indicated in the product labeling, resulting in syringe detection and infusion accuracy that can result in delays in therapy, overinfusion, or underinfusion.
Device Classification20220330
Device Code InfoSerial Numbers: 633299, 633307, 633310, 633313, 633315, 633318 GUIDID: 04046963716745
Center Classification Date20220322
Recall Initiation Date20220207
Recalling FirmB Braun Medical Inc
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.