Reported Oct 30, 2024 · Ongoing
CADD Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24
Smiths Medical ASD Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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 Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24
- Lot codes and dates
- UDI/DI 10610586027215
- Lot Numbers
4042839404024840340214052405403402240377484042841403401940377494040247398333939833383983340401336740133663988532-ENG39833374052406404284040524074052408404284240488914052409
- Amount recalled
- 119535 units
This recall covers 14 products
The agency filed one notice per product. You are reading one of them; the other 13 are below.
1 more are in the archive.
Why it was recalled
Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Smiths Medical ASD Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.