Reported Mar 11, 2026 · Ongoing
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A…
B Braun Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B Braun Medical Inc · 824 12th Ave · Bethlehem, PA · 18018-3524
Is this the product you have?
- Brand NameB
- Braun Product Name21GA WINGED INFUSION
- SINGLE PK Model/Catalog Number7A3842
- Software VersionN/A
- Product DescriptionA device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids
- ComponentN/A
- Lot codes and dates
9 of 9 products
Products covered by this recall Model / number Barcodes Product as published 7A3842Model/ — 4046964338434Primary-DI 4046964338434 — 4046964338410Unit 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 - Amount recalled
- 21000 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
- TX
Why it was recalled
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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