Graseby 3300 Pump and Graseby 3000 Series Pump Accessories Patient controlled syringe pump. Use for Infusion
Reported: February 7, 2018 Initiated: August 24, 2017 #Z-0497-2018
Product Description
Graseby 3300 Pump and Graseby 3000 Series Pump Accessories Patient controlled syringe pump. Use for Infusion
Reason for Recall
In certain cases, the lock and key supplied with Graseby 3300 pumps and accessories does not match the standard Graseby 3300 key.
Details
- Recalling Firm
- Smiths Medical ASD Inc.
- Units Affected
- 77
- Distribution
- Worldwide Distribution to the countries of : Australia, Canada, Germany, France, Great Britain, Hong Kong, and Ireland
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
Graseby 3300 Pump and Graseby 3000 Series Pump Accessories Patient controlled syringe pump. Use for Infusion. Recalled by Smiths Medical ASD Inc.. Units affected: 77.
Why was this product recalled? ▼
In certain cases, the lock and key supplied with Graseby 3300 pumps and accessories does not match the standard Graseby 3300 key.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 7, 2018. Severity: Moderate. Recall number: Z-0497-2018.
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