Smiths Medical recalls certain CADD medication cassette reservoirs with weakened bag welds that may cause medication leakage. Affected units include specific lot numbers and product codes. Contact for remedy.
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, potentially causing leakage. This could lead to medication being spilled during use, which might affect treatment safety.
Weakened welds along the bag perimeter inside the reservoir housing may cause medication to leak out. This leakage could lead to medication being spilled during use, potentially affecting treatment safety.
Healthcare professionals using these reservoirs for medication delivery are most at risk. Patients receiving treatment with affected units could experience medication leakage.
Check for product code 21-7002-24, lot numbers 6022010 through 6063845, or UDI/DI 10610586022128. The reservoirs are 100mL and include a clamp and female Luer connector.
Identify the product code (21-7002-24), lot numbers (6022010-6063845), or UDI/DI (10610586022128) to confirm if your reservoir is affected.
Certain CADD medication cassette reservoirs may have weakened welds along the bag perimeter, which could cause medication leakage during use.
Check the product code, lot numbers, or UDI/DI to see if your reservoir is affected. The recall does not specify a remedy for affected units.
The recall states medication leakage is possible, but no specific risk of serious injury is mentioned. This is considered a low-risk hazard.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2523-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-2523-2025 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.
