FDA Device recall Z-2132-2024

Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260

FDA Device
Class II
ongoing
Published 2024-06-19

On 2024-06-19 the FDA classified a Class II recall of Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260 by B Braun Medical, citing the devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2132-2024
Classification	Class II
Status	ongoing
Initiated	2024-05-17
Published	2024-06-19
Last updated	2026-09-13 11:57 UTC
Company	B Braun Medical
Distribution	US

Product

Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260

Reason

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

Identifiers

code_info	Catalogue Number: 4894260; UDI/DI: 04022495101211; Lot/Batch: 22E07, 20E08, 20E09, 23E09, 23E10, 19E11, 23E11, 23E13, 1… Catalogue Number: 4894260; UDI/DI: 04022495101211; Lot/Batch: 22E07, 20E08, 20E09, 23E09, 23E10, 19E11, 23E11, 23E13, 19E14, 20E14, 19E15, 19E16, 23E17, 23E18, 23E20, 22E21, 21E25, 22E25, 22E27, 20E29, 19E30, 20E30, 19E31, 22E31, 19F04, 19F05, 19F07, 19F21, 19F22, 19F26, 19F27, 19F28, 19F29, 19G30, 19H01, 19H02, 19H07, 19H08, 19H31, 19I04, 19I06, 19I07, 19K01, 19K02, 19K04, 19K08, 19K09, 19K27, 19K30, 19L06, 19L07, 19M05, 19M07, 19M10, 20A09, 20A11, 20A15, 20A17, 20B05, 20B06, 20B08, 20C03, 20C04, 20C05, 20C07, 20C11, 20C12, 20C20, 20C25, 20C26, 20C27, 20D07, 20D08, 20D09, 20D22, 20D23, 20D24, 20D28, 20F02, 20F03, 20F05, 20F20, 20F23, 20F25, 20F26, 20F27, 20F30, 20G01, 20G09, 20G10, 20G14, 20G15, 20G16, 20G17, 20H06, 20H08, 20H18, 20H19, 20H20, 20I04, 20I09, 20I11, 20I12, 20I30, 20K02, 20K03, 20K10, 20K14, 20K16, 20L06, 20L07, 20L12, 20L14, 20L18, 20M09, 20M11, 20M12, 21A06, 21A08, 21A09, 21A13, 21A15, 21A21, 21A27, 21A28, 21A30, 21B16, 21B27, 21C03, 21C04, 21C06, 21C20, 21C24, 21C25,

code_info

Catalogue Number: 4894260; UDI/DI: 04022495101211; Lot/Batch: 22E07, 20E08, 20E09, 23E09, 23E10, 19E11, 23E11, 23E13, 1…

Catalogue Number: 4894260; UDI/DI: 04022495101211; Lot/Batch: 22E07, 20E08, 20E09, 23E09, 23E10, 19E11, 23E11, 23E13, 19E14, 20E14, 19E15, 19E16, 23E17, 23E18, 23E20, 22E21, 21E25, 22E25, 22E27, 20E29, 19E30, 20E30, 19E31, 22E31, 19F04, 19F05, 19F07, 19F21, 19F22, 19F26, 19F27, 19F28, 19F29, 19G30, 19H01, 19H02, 19H07, 19H08, 19H31, 19I04, 19I06, 19I07, 19K01, 19K02, 19K04, 19K08, 19K09, 19K27, 19K30, 19L06, 19L07, 19M05, 19M07, 19M10, 20A09, 20A11, 20A15, 20A17, 20B05, 20B06, 20B08, 20C03, 20C04, 20C05, 20C07, 20C11, 20C12, 20C20, 20C25, 20C26, 20C27, 20D07, 20D08, 20D09, 20D22, 20D23, 20D24, 20D28, 20F02, 20F03, 20F05, 20F20, 20F23, 20F25, 20F26, 20F27, 20F30, 20G01, 20G09, 20G10, 20G14, 20G15, 20G16, 20G17, 20H06, 20H08, 20H18, 20H19, 20H20, 20I04, 20I09, 20I11, 20I12, 20I30, 20K02, 20K03, 20K10, 20K14, 20K16, 20L06, 20L07, 20L12, 20L14, 20L18, 20M09, 20M11, 20M12, 21A06, 21A08, 21A09, 21A13, 21A15, 21A21, 21A27, 21A28, 21A30, 21B16, 21B27, 21C03, 21C04, 21C06, 21C20, 21C24, 21C25,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2132-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.