Smiths Medical recalls 50mL medication cassette reservoirs with weakened welds that could cause medication leakage. Affected units include 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 certain 50mL 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 may cause medication to leak. This leakage could potentially lead to medication exposure or contamination during medical procedures.
Healthcare professionals using these reservoirs for medication administration are most at risk. Patients receiving medication through these reservoirs could be affected if leakage occurs.
Check for product code 21-7001-24, lot numbers 6022008, 6022009, 6037749, 6062686, or 6062687. These reservoirs were sold with a nonvented stopper and female Luer connector.
Verify your reservoir's product code and lot numbers to confirm if it's affected.
The recall does not require immediate stoppage; affected units should be checked for the specific lot numbers and product code.
Leakage could occur if the welds weaken, potentially leading to medication exposure during medical procedures.
Check for product code 21-7001-24 and lot numbers 6022008, 6022009, 6037749, 6062686, or 6062687.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2522-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-2522-2025 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.
