FDA recall Z-0252-2020

Product

BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608

Reason for recall

BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.

Distribution

Distributed to accounts in AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, and VA. Foreign distribution to Canada, Brazil, India, Mexico, Singapore, and Taiwan.

Key facts

Status

Terminated

Initiation date

2019-03-07

Report date

2019-11-06

Termination date

2022-02-11

Voluntary/Mandated

Voluntary: Firm initiated

Location

Franklin Lakes, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0252-2020