Smiths Medical recalls certain CADD 50mL and 100mL medication cassette reservoirs with weakened welds that could cause medication leakage. Affected units have specific lot numbers and product codes.
Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
Smiths Medical is recalling some medication cassette reservoirs that may have weakened welds around the medication bag. This could lead to medication leakage, which might affect patient safety during medical treatments.
Weakened welds along the bag perimeter inside the plastic housing could cause medication to leak around the reservoir. This leakage might lead to contamination or inaccurate dosing during medical procedures.
Healthcare professionals using these reservoirs in medical settings are most at risk. Patients receiving medication through these devices could be affected if leakage occurs.
Check for product codes 21-7302-24 and lot numbers listed in the recall notice. These reservoirs are sold in 100mL sizes with a non-vented stopper.
Verify the product code (21-7302-24) and lot numbers (4468669 to 6062723) to confirm if your reservoir is affected.
Certain CADD 50mL and 100mL medication cassette reservoirs may have weakened welds along the bag perimeter, which could cause medication leakage.
Check the product code and lot numbers listed in the recall notice to determine if your reservoir is affected. If it is, contact Smiths Medical for further instructions.
Look for product code 21-7302-24 and lot numbers from 4468669 to 6062723. These specific units are part of the recall.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2526-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-2526-2025 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.
