Smiths Medical recalls certain CADD medication cassette reservoirs (50mL/100mL) that may leak medication due to weakened welds. 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 could leak medication because of weak welds around the bag. This might cause medication to spill, which could be a problem for patients using these devices.
The reservoirs may have weakened welds along the bag's edge inside the plastic housing. This could cause medication to leak around the perimeter of the bag, potentially leading to spills.
Healthcare providers using these reservoirs for medication delivery are most at risk. Patients receiving treatment with these devices could be affected if the reservoir leaks.
Check for product codes 21-7301-24, lot numbers listed in the recall, or UDI/DI 10610586027215. These reservoirs are used in medical settings for medication delivery.
Verify your reservoir's product code (21-7301-24) and lot numbers (6005583-6092859) to confirm if it's affected.
The reservoirs may have weakened welds along the bag perimeter, which could cause medication leakage.
The recall does not specify a remedy, so check the product details to see if it's affected and contact Smiths Medical for further guidance.
Leakage of medication could occur, but the recall indicates low risk as the hazard is not severe enough to cause serious injury.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2525-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-2525-2025 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.
