Reported Feb 8, 2023 · Ongoing
CADD Administration Set, List Numbers: a) REF 21-7308-24, b) REF 21-7309-24, c) REF 21-7310-24, d) REF 21-7308-24JP, e)…
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 Numbersa) REF 21-7308-24, b) REF 21-7309-24, c) REF 21-7310-24, d) REF 21-7308-24JP, e) REF 21-7309-24JP. Computerized Ambulatory Delivery Device
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Barcodes Product as published 21-7308-2430610586032374UDI/DI 30610586032374, Lot Numbers: 4053922 through 4334076 21-7309-2430610586032381UDI/DI 30610586032381, Lot Numbers: 4062405 through 4334085 21-7310-2430610586032398UDI/DI 30610586032398, Lot Numbers: 4062404 through 4330874 21-7308-24JPUDI/DI N/A, Lot Numbers: 4053922 through 4334075 21-7309-24JPUDI/DI N/A, Lot Numbers: 4062405 through 4330870. - Amount recalled
- 726,878 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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