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B. Braun Medical, Inc. Recall 92523

Description: Design Options¿ / Epidural anesthesia kit (10 count carton)

B. Braun Medical, Inc. Recall 92523 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-2003-2023
Event ID92523
Event DescriptionDesign Options¿ / Epidural anesthesia kit (10 count carton)
Product TypeDevices
DistributionUS Nationwide distribution.
Quantity3,560 units
Recall ReasonKits were assembled with the incorrect Filter Straw.
Device Classification20230705
Device Code InfoModel No. 552177, 552155, 552179, 552116; GTIN: 04046955596102, 04046955214440, 04046955596140, 04046964950254; Lot No. 0061853751, 0061854949, 0061855598, 0061855133.
Center Classification Date20230623
Recall Initiation Date20230605
Recalling FirmB. Braun Medical, Inc.
Initial Notification Letter
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