Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes
Reported: April 22, 2020 Initiated: January 7, 2020 #Z-1716-2020
Product Description
Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes
Reason for Recall
Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have broken luers.
Details
- Recalling Firm
- Smiths Medical ASD, Inc.
- Units Affected
- 127,700 total devices
- Distribution
- USA: AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI,MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA. Int'l: CA, DE, AU.
- Location
- Keene, NH
Frequently Asked Questions
What product was recalled? ▼
Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes. Recalled by Smiths Medical ASD, Inc.. Units affected: 127,700 total devices.
Why was this product recalled? ▼
Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have broken luers.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 22, 2020. Severity: Moderate. Recall number: Z-1716-2020.
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