Home / Recalls / B Braun Medical Inc / Z-2133-2024

Z-2133-2024 Class II Ongoing

Recalled by B Braun Medical Inc — Breinigsville, PA

Recall Details

Product Type
Devices
Report Date
June 19, 2024
Initiation Date
May 17, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
108,811 units

Product Description

Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278

Reason for Recall

The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.

Distribution Pattern

Worldwide distribution - US Nationwide and the country of Canada.

Code Information

Catalogue Number: 4894278; UDI/DI: 04022495101266; Lot/Batch: 20E15, 21E18, 19F08, 19G10, 19G13, 19G19, 19I19, 20C28, 20C31, 20D10, 20L19, 21B13, 21I17, 21K21, 21L12, 21M16, 22D12, 22H20, 22I22, 22K27, 23A20, 23C04, 23D14, 23F09, 23I08, 23I29,

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