Smiths Medical Medfusion Guide Barrel Clamp, Item number G6000716
Reported: April 24, 2024 Initiated: December 19, 2023 #Z-1543-2024
Product Description
Smiths Medical Medfusion Guide Barrel Clamp, Item number G6000716
Reason for Recall
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.
Details
- Recalling Firm
- Smiths Medical ASD Inc.
- Units Affected
- 1842 guide barrel clamps
- Distribution
- Worldwide distribution.
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
Smiths Medical Medfusion Guide Barrel Clamp, Item number G6000716. Recalled by Smiths Medical ASD Inc.. Units affected: 1842 guide barrel clamps.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 24, 2024. Severity: Moderate. Recall number: Z-1543-2024.
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