Reported May 27, 2026 · Ongoing
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…
Becton, Dickinson and Company
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: Becton, Dickinson and Company · 17200 Laguna Canyon Rd · Irvine, CA · 92618-5403
Is this the product you have?
- Swan-Ganz Catheter
- Models
131F7/131F7P131F7J141F7151F7834F75096F6/096F6PC144F7782F75M132F5C146F7831F75/831F75PTS105F5774F75777F8AIQSGF8
- Lot codes and dates
- Model/UDI-DI/Lot(Expiration)
655 of 655 codes
131F7P/00690103000412/65902900(8/1/2026)65902901(8/3/2026)65910728(8/2/2026)65910729(7/29/2026)65910730(7/27/2026)65910731(7/25/2026)65910732(7/26/2026)65910735(7/30/2026)65910736(8/24/2026)65910737(7/31/2026)65916927(8/3/2026)65916928(8/6/2026)65916929(8/7/2026)65916930(8/8/2026)65916931(8/9/2026)65916932(8/22/2026)65916933(8/23/2026)65944791(8/20/2026)65944792(8/21/2026)65955857(9/9/2026)65955858(9/17/2026)65955859(9/26/2026)65955860(9/27/2026)65973739(9/5/2026)65973740(9/6/2026)65973741(9/7/2026)65973742(9/10/2026)65988571(9/28/2026)65997478(9/16/2026)65997479(9/17/2026)65997481(9/19/2026)65997482(9/20/2026)66010504(9/10/2026)66010505(9/11/2026)66010506(9/12/2026)66010507(9/13/2026)66010508(9/14/2026)66023074(9/30/2026)66033088(10/5/2026)66048930(10/9/2026)66057629(10/6/2026)66057630(10/8/2026)66057944(10/15/2026)66057945(10/17/2026)66061552(10/24/2026)66074999(10/4/2026)66075318(11/19/2026)66104892(10/21/2026)66104893(10/22/2026)66104894(10/23/2026)66104895(11/13/2026)66108277(11/15/2026)66118638(11/22/2026)66120310(10/29/2026)66120312(10/30/2026)66120313(10/31/2026)66127027(11/15/2026)66127028(11/20/2026)66132570(11/21/2026)66132571(11/25/2026)
- Model/UDI-DI/Lot(Expiration)
- Amount recalled
- 589,223
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
Why it was recalled
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
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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