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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98380

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

Open FDA event record

Event summary

Timeline bucket
February 02, 2026
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

3 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 3

Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A

Z-1481-2026
Recall number
Z-1481-2026
Initiated
February 02, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
105550 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

Code information

Model/Catalog Number: 7B3050; Primary-DI 4046964341298, Unit of Use- DI 4046964341274; Lot 0062006430, Exp 30APR2032; Lot 0062006470, Exp 30JUN2032; Lot 0062006471, Exp 31MAY2032; Lot 0062014964, Exp 31JUL2032; Lot 0062014965, Exp 31JUL2032; Lot 0062014966, Exp 30SEP2032; Lot 0062027579, Exp 31AUG2032.

Distribution pattern

Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.

device · product 2 of 3

Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A

Z-1482-2026
Recall number
Z-1482-2026
Initiated
February 02, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
21000 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

Code information

Model/Catalog Number: 7A3842; Primary-DI 4046964338434; Unit of Use- DI 4046964338410; Lot 0062004706, Exp 31MAR2032; Lot 0062005799, Exp 30JUN2032; Lot 0062006415, Exp 31MAR2032; Lot 0062006416, Exp 31MAR2032; Lot 0062023397, Exp 30JUN2032; Lot 0062024887, Exp 31JUL2032

Distribution pattern

Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.

device · product 3 of 3

Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A

Z-1483-2026
Recall number
Z-1483-2026
Initiated
February 02, 2026
Classification
Class II
Status
Ongoing
Recalling firm
B Braun Medical Inc
Quantity
51300 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

Code information

Model/Catalog Number: 7M2802; Primary-DI 4046964787102, Unit of Use- DI 4046964349904; Lot 0062003864, Exp 30APR2032; Lot 0062004133, Exp 30JUN2032; Lot 0062006454, Exp 31JUL2032; Lot 0062028929, Exp 31AUG2032; Lot 0062037141, Exp 30SEP2032, Lot 0062037691, Exp 30SEP2032.

Distribution pattern

Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica.