Smiths Medical ASD, Inc. - 4000-0105-78
Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded.
Smiths Medical ASD, Inc. - 4000-0105-78
This product is a low-risk medical device. It is designed for use in healthcare settings and is intended to be safe for patients and healthcare providers.
All
Check the product's serial numbers and UDI/DI to ensure they match the provided information. Verify that the product is within the expected range of serial numbers for the specific model.
Confirm the product's UDI/DI and serial numbers match the provided information.
Ensure the product is within the expected range of serial numbers for the specific model.
Verify that the product is intended for use in healthcare settings and is safe for patients and healthcare providers.
The UDI/DI for this product is 10610586043574.
The serial numbers for this product are: 2026172, 2026433, 2032847, 2032881, 2033072, 2033132, 2035215, 2035443, 2035448, 2035454, 2035457, 2035458, 2035501, 2036239, 2036483, 2036494, 2036626
Yes, this product is a low-risk medical device designed for use in healthcare settings and is intended to be safe for patients and healthcare providers.
We’ve drafted a message you can send Smiths Medical ASD, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-1541-2024 — Smiths Medical ASD, Inc. Smiths Medical ASD, Inc. Hello, I own a Smiths Medical ASD, Inc. that is covered by recall Z-1541-2024 from Smiths Medical ASD, Inc.. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.