Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
Reported: August 15, 2018 Initiated: April 13, 2018 #Z-2662-2018
Product Description
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
Reason for Recall
Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the size of a loaded syringe.
Details
- Recalling Firm
- Smiths Medical ASD Inc.
- Units Affected
- 276 units
- Distribution
- US distribution to AL, AZ, CA, DC, FL, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NJ, NM, NY, OH, OK, PA, TN, TX, UT, VA, WA. International distribution to Canada and Lebanon.
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism. Recalled by Smiths Medical ASD Inc.. Units affected: 276 units.
Why was this product recalled? ▼
Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the size of a loaded syringe.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 15, 2018. Severity: Moderate. Recall number: Z-2662-2018.
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