Smiths Medical recalls certain CADD Medication Cassette Reservoirs (100mL) due to potential medication leakage from weakened weld joints. 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 100mL CADD Medication Cassette Reservoirs 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 during use, potentially leading to incorrect dosing if the reservoir leaks.
Healthcare professionals using these reservoirs for medication delivery are most at risk. Patients receiving treatment with these reservoirs could experience medication errors.
Check for product code 21-7002-24 and lot numbers 3977441, 4013370, 3983314, 4013371, 4013369, 4013372, 4025948, 4033993, 4037444, or 4040238 on the reservoir packaging.
Look for product code 21-7002-24 and the listed lot numbers on the reservoir packaging.
A production equipment malfunction may create a weakened weld joint between the medication bag and tubing, which could cause medication leakage.
Check the product code and lot numbers on the packaging. If it matches the recalled items, contact Smiths Medical for further instructions.
The recall is for potential medication leakage, which could lead to incorrect dosing, but no specific injury risk is mentioned in the notice.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0010-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-0010-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
