Smiths Medical ASD Inc. 2024-08-14 Health critical FDA
Health · FDA · Recall #FDA-Z-2421-2024
CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21-2120 , 21-2125 , and… Recall
Issued August 14, 2024 · Smiths Medical ASD Inc.
In August 2024, Smiths Medical ASD Inc. recalled the CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21-2120 , 21-2125 , and…, 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
The CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses: " For intravenous, intraarterial, subcutaneous, intraperitoneal, perineural, surgical site, epidural space, or subarachnoid space infusion.
What you should do
- 1 Stop using CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21-2120 , 21-2125 , and… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Smiths Medical ASD 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
- Smiths Medical ASD Inc.
- Category
- Health
- Recall date
- August 14, 2024
- Units affected
- Not reported
- Sold at
- Worldwide
- Recall number
- FDA-Z-2421-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Smiths Medical ASD Inc. has 4 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.