Reported Feb 8, 2023 · Ongoing
CADD Administration Set, List Numbers
Smiths Medical ASD Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.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: Smiths Medical ASD Inc. · 6000 Nathan Ln N · Minneapolis, MN · 55442-1690
Is this the product you have?
CADD Administration Set, List Numbers
24 of 24 products
| Model / number | Product as published |
|---|---|
21-7300-24 | — |
21-7301-24 | — |
21-7302-24 | — |
21-7321-24 | — |
21-7322-24 | — |
21-7323-24 | — |
21-7324-24 | — |
21-7333-24 | — |
21-7336-24 | — |
21-7339-24 | — |
21-7343-24 | — |
21-7349-24 | — |
21-7359-24 | — |
21-7383-24 | — |
21-7390-24 | — |
21-7391-24 | — |
21-7394-24 | — |
21-7395-24 | — |
21-7301-24JP | — |
21-7302-24JP | — |
- Amount recalled
- 45285351 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Stop using this product now
There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False "No Disposable Attached (NDA)" Alarms
Using this product could cause serious injury, illness or death — stop using it now.
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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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