Angiodynamics, Inc. 2024-05-15 Health serious FDA
Health · FDA · Recall #FDA-Z-1762-2024
DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Term… Recall
Issued May 15, 2024 · Angiodynamics, Inc.
In May 2024, Angiodynamics, Inc. recalled the DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Term…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
What you should do
- 1 Stop using DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Term… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Angiodynamics, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Angiodynamics, Inc.
- Category
- Health
- Recall date
- May 15, 2024
- Units affected
- Not reported
- Sold at
- VA
- Recall number
- FDA-Z-1762-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Angiodynamics, Inc. has 9 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.