Smiths Medical recalls CADD Medication Cassette Reservoirs (50mL, Product Code 21-7001-24) due to potential medication leakage from weakened weld joints. Affected units include specific 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 CADD Medication Cassette Reservoirs (50mL) because they may have weakened weld joints that could cause medication leakage. This poses a risk of incorrect medication dosing if the reservoir leaks during use.
The reservoirs may have a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could lead to medication leakage, potentially causing incorrect dosing if the reservoir leaks during use.
Healthcare professionals using these reservoirs for medication administration are likely affected. Patients receiving medication through these reservoirs could be at risk if leakage occurs.
Check for the product code 21-7001-24 and lot numbers 4040237, 4013368, 3983342, 4046817, 405240, or 4060903. These units were sold with the UDI/DI 10610586022111.
Identify the product code and lot numbers to confirm if your reservoir is affected.
Smiths Medical recalls these reservoirs because a production equipment malfunction may cause weakened weld joints, leading to medication leakage.
The recall does not specify a remedy, so check the product details to see if it is affected and contact Smiths Medical for further instructions.
Yes, affected units include lot numbers 4040237, 4013368, 3983342, 4046817, 405240, and 4060903.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0014-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0014-2025 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.
