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 / numberBarcodesProduct 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.

Want the full recall guide?

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:39 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.