OriGen recalls 32Fr Reinforced Dual Lumen Cannulas (REF: VV3: VV32F) due to potential barium sulfate omission and incorrect tip length. This affects medical use in extracorporeal life support.
These catheters may have the following deficiencies: 1) barium sulfate omission, and 2) actual catheter tip length is one centimeter shorter than printed on the tip
OriGen is recalling its Reinforced Dual Lumen Cannulas (32Fr, REF: VV32F) because they may lack barium sulfate and have a shorter tip than labeled. This could cause issues during critical medical procedures like extracorporeal life support.
The cannulas may lack barium sulfate, which is a critical component for certain medical procedures. Additionally, the tip is one centimeter shorter than printed, which could lead to improper placement in the body.
Healthcare professionals using these cannulas for extracorporeal life support procedures are most at risk. Patients receiving this treatment may be affected if the cannula is used incorrectly.
Check for the model number REF: VV32F on the packaging or label. The cannulas are sterile and intended for extracorporeal life support procedures.
Look for the model number REF: VV32F on the packaging or label to confirm if it is recalled.
The cannulas may have barium sulfate omission and the tip length is one centimeter shorter than printed on the label.
The risk includes potential improper placement due to the shorter tip length and possible lack of barium sulfate, which could affect medical procedures.
Check for the model number REF: VV32F on the packaging or label. The cannulas are sterile and intended for extracorporeal life support procedures.
We’ve drafted a message you can send OriGen to request your refund or repair — edit it as you like.
Subject: Recall Z-0184-2019 — OriGen OriGen Hello, I own a OriGen that is covered by recall Z-0184-2019 from OriGen. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
