Smiths Medical recalls 100mL CADD Medication Cassette Reservoirs with weak weld joints that may cause medication leakage. Affected units have specific product codes and lot numbers.
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.
Smiths Medical is recalling certain 100mL medication cassette reservoirs that may have a weakened weld joint, potentially causing medication leakage. This could lead to improper medication delivery if the reservoir leaks.
A production equipment malfunction may cause a weakened weld joint between the medication bag and tubing. This could result in medication leakage, potentially affecting the accuracy of medication delivery.
Healthcare professionals using these reservoirs for medication delivery are likely affected. Patients receiving medication through these reservoirs are at risk if the reservoir leaks.
Check for product code 21-7302-24 and lot numbers listed in the recall notice. The reservoirs are 100mL, FS (for use with specific medical devices), and have specific UDI/DI numbers.
Identify the product code (21-7302-24) and lot numbers from the recall list to confirm if your reservoir is affected.
Certain CADD Medication Cassette Reservoirs may have a weakened weld joint between the medication bag and tubing, which could cause medication leakage.
Check for product code 21-7302-24 and lot numbers listed in the recall notice (e.g., 3971709, 3983317, etc.).
The recall does not specify a remedy, so contact Smiths Medical for guidance on next steps.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0011-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0011-2025 from Smiths Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
