Smiths Medical recalls certain CADD Medication Cassette Reservoirs (50mL) due to weakened 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 some CADD Medication Cassette Reservoirs (50mL) because a production issue might cause medication leakage. This could lead to incorrect dosing if the reservoir leaks during use.
A production equipment malfunction may create a weakened weld joint between the medication bag and tubing. This could cause medication leakage, potentially leading to incorrect dosing if the reservoir leaks during use.
Healthcare professionals using these reservoirs for medication delivery are most at risk. Patients receiving treatments through these reservoirs could be affected if the leak occurs.
Check for the product code 21-7301-24 and lot numbers listed in the recall notice (e.g., 4042839, 4040248). These reservoirs are sold for medical use in hospitals and clinics.
Verify the product code (21-7301-24) and lot numbers (e.g., 4042839) to confirm if your reservoir is affected.
A production equipment malfunction may cause weakened weld joints between the medication bag and tubing, potentially leading to medication leakage.
Check the product code and lot numbers listed in the recall notice to confirm if your reservoir is affected. No immediate action is required if it's not affected.
The recall is for possible medication leakage, which could lead to incorrect dosing. However, the hazard does not indicate a risk of serious injury in normal use.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0013-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0013-2025 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.
