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FDA (Device enforcement)Recalled 2024-05-17class ii

B Braun Medical Inc: Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278

Hazard

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

Details from the source

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: Worldwide distribution - US Nationwide and the country of Canada. Quantity: 108,811 units Lot/code info: 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,

UPC codes

04022495101266

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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