Cardinal Health 200, LLC 2024-02-28 Health critical FDA
Health · FDA · Recall #FDA-Z-1045-2024
Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, NEEDLE PORT, 16 FR (5.3 MM), 5 CC, 2000 ML… Recall
Issued February 28, 2024 · Cardinal Health 200, LLC
In February 2024, Cardinal Health 200, LLC recalled the Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, NEEDLE PORT, 16 FR (5.3 MM), 5 CC, 2000 ML…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
What you should do
- 1 Stop using Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, NEEDLE PORT, 16 FR (5.3 MM), 5 CC, 2000 ML… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Cardinal Health 200, LLC 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
- Cardinal Health 200, LLC
- Category
- Health
- Recall date
- February 28, 2024
- Units affected
- Not reported
- Sold at
- US and EMEA, Japan, Latin America
- Recall number
- FDA-Z-1045-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Cardinal Health 200, LLC has 12 recalls in our database, including 4 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.