Bard Peripheral Vascular Inc recalls TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bone Marrow Aspiration

Recalled August 18, 2021 · FDA recall Z-2249-2021 · Bard Peripheral Vascular

Hazard

Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile. · FDA Class II

Units

1,200 device

Sold at

U.S Nationwide Distribution in the states of .: AZ, CT, DC, FL, IL, MA, MI, MO, NY, OK, TX, and VA O.U.S.: Australia, Belgium, China, EMEA, Japan, Mexico, Saudi Arabia, Singapore, Taiwan

Description

Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.

Product

TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 15G x 79mm

Manufacturer(s)

Bard Peripheral Vascular Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →