Bard Peripheral Vascular Inc: Medical Device Recall in 2021 - (Recall #: Z-2249-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 23, 2021

Date Posted: August 18, 2021

Recall Number: Z-2249-2021

Event ID: 88314

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1,200 device

Code Information:

Catalog Number/UDI: TIN3018/(01)10885403043819(17)241031(10)0001330956; TIN3015/(01)10885403043796(17)241031(10)0001331229; Serial Numbers: 0001330956; 0001331229;

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated