Smiths Medical recalls yellow-striped CADD medication reservoirs with potential medication leakage due to weakened welds. 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 yellow-striped medication reservoirs that may leak medication due to weakened welds. This could lead to medication exposure or contamination if the reservoirs are used improperly.
Weakened welds along the perimeter of the medication bag inside the reservoir could cause medication to leak. This leakage might lead to medication exposure or contamination if the reservoir is used without proper containment.
Healthcare professionals using these reservoirs in medical settings are most at risk. Patients receiving medication through these reservoirs could be affected if leaks occur.
Check for yellow-striped tubing, the product code 21-7600-24, and lot numbers 6037784 or 6054015. The reservoirs have a yellow stopper and come with a female NRFit connector.
Verify the product code (21-7600-24) and lot numbers (6037784, 6054015) to confirm if your reservoir is affected.
Certain CADD 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 could lead to medication exposure or contamination, but the risk is low as the issue is limited to specific units.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2527-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-2527-2025 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.
