FDA-Device2022-02-02Class II
PIVO Blood Collection Device 20G, REF: 202-0005
Velano Vascular
Hazard
Incomplete sealing of blood collection device unit packages may produce a breach in the sterile barrier enclosing the product. This could lead to microbial contamination of the device prior to use. The health effects range from no clinical effect up to bloodstream infection.
Sold states
US Nationwide distribution in the states of CT, CO, UT, PA, IL, WA, CA, NJ, MI, FL, NC.
Affected count
123,700
Manufactured in
221 Pine St # 200, San Francisco, CA, United States
Products
PIVO Blood Collection Device 20G, REF: 202-0005
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0527-2022Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief