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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94637

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 17, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
B Braun Medical Inc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 4

Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.

Z-2131-2024
Recall number
Z-2131-2024
Initiated
May 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
20,850 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Catalogue Number: 4894251; UDI/DI: 04022495101167; Lot/Batch: 20E15, 19L09, 19L27, 20A19, 20H21, 21G14, 21I16, 22H23,

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 2 of 4

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

Z-2132-2024
Recall number
Z-2132-2024
Initiated
May 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
1,783,991 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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, 21C27, 21C31, 21D15, 21D17, 21D20, 21F11, 21F12, 21F16, 21F17, 21G01, 21G02, 21G03, 21G07, 21G27, 21G28, 21G29, 21G31, 21H03, 21H11, 21H13, 21H20, 21I09, 21I11, 21I14, 21I15, 21I29, 21I30, 21K01, 21K02, 21K06, 21K15, 21K16, 21K20, 21K22, 21K23, 21K27, 21K28, 21L06, 21L07, 21L09, 21L10, 21L23, 21L25, 21L26, 21L27, 21M04, 21M07, 21M08, 21M09, 21M18, 21M21, 21M22, 21M24, 22A12, 22A14, 22A15, 22B04, 22B08, 22B09, 22B16, 22B17, 22C05, 22C09, 22C10, 22C12, 22D05, 22D07, 22D22, 22D26, 22D28, 22D29, 22F16, 22F18, 22F22, 22F24, 22G02, 22G06, 22G08, 22G12, 22H04, 22H06, 22H10, 22H11, 22H19, 22I10, 22I13, 22I15, 22I21, 22K06, 22K08, 22K12, 22K13, 22K14, 22K25, 22K26, 22K27, 22L06, 22L08, 22L09, 22L10, 22M08, 22M10, 22M13, 22M24, 22M28, 23A13, 23B15, 23B17, 23C07, 23C08, 23C10, 23C14, 23C31, 23D04, 23D05, 23D12, 23D14, 23F20, 23F22, 23F23, 23G12, 23G14, 23G19, 23G20, 23G22, 23G25, 23G26, 23H05, 23H09, 23H11, 23H18, 23H20, 23H23, 23H24, 23H25, 23I13, 23I14, 23I15, 23I16, 23I21, 23K05, 23K06, 23K11,

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 3 of 4

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

Z-2133-2024
Recall number
Z-2133-2024
Initiated
May 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
108,811 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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,

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 4 of 4

Stimuplex A, 30 DEG, 22GX2", 0.70x50mm, Catalogue Number: 4894502

Z-2134-2024
Recall number
Z-2134-2024
Initiated
May 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
1,157,640 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component design/selection

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Catalogue Number: 4894502; UDI/DI: 04022495101310; Lot/Batch: 20E01, 20E03, 21E07, 21E09, 19E10, 22E10, 22E11, 21E13, 20E19, 20E20, 19E21, 19E22, 20E22, 23E26, 20E27, 23E31, 19F12, 19F13, 19F15, 19G03, 19G04, 19G06, 19G09, 19G20, 19G21, 19G24, 19G25, 19G27, 19H23, 19H28, 19H30, 19I11, 19I21, 19I25, 19I26, 19K11, 19K16, 19K17, 19K24, 19K25, 19L12, 19L13, 19L15, 19L19, 19M12, 19M14, 19M17, 19M21, 19M24, 19M26, 20A30, 20A31, 20B15, 20B18, 20B19, 20B21, 20B26, 20B27, 20C14, 20C17, 20C18, 20D01, 20D02, 20D04, 20D14, 20D16, 20D17, 20D21, 20D29, 20F06, 20F10, 20F11, 20F12, 20F13, 20G21, 20G22, 20G23, 20G29, 20G31, 20H01, 20H05, 20H26, 20H27, 20H29, 20L27, 20L28, 20M03, 20M19, 20M23, 20M25, 20M26, 21A16, 21A19, 21B04, 21B06, 21B10, 21B18, 21B20, 21B25, 21C11, 21C13, 21C17, 21D07, 21D08, 21D10, 21D29, 21F19, 21F23, 21F24, 21F25, 21F26, 21F30, 21G08, 21G09, 21G10, 21G14, 21G17, 21G20, 21G21, 21H05, 21H06, 21H07, 21H26, 21H28, 21I04, 21I22, 21I26, 21K07, 21K09, 21K13, 21K29, 21K30, 21L16, 21L17, 21L18, 21L19, 21L20, 21L30, 21M02, 21M03, 21M11, 21M14, 22A08, 22A25, 22B25, 22B27, 22C02, 22C03, 22C25, 22C29, 22D14, 22D15, 22D19, 22D21, 22F02, 22F04, 22G14, 22G16, 22G21, 22G23, 22G29, 22H25, 22I01, 22I03, 22I08, 22I28, 22K01, 22K05, 22K16, 22K18, 22K19, 22K20, 22L01, 22L02, 22L15, 22L16, 22M06, 22M15, 22M17, 23A08, 23A11, 23A31, 23B01, 23B07, 23B25, 23B28, 23C16, 23C18, 23C21, 23D19, 23D22, 23D28, 23F07, 23F30, 23G07, 23G11, 23G29, 23H01, 23I05, 23I06, 23I07, 23I23, 23I26, 23I28, 23I29, 23K18, 23K19,

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.