Dynarex Corporation: Medical Device Recall in 2016 - (Recall #: Z-2057-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product Usage:containers for sample collection

Product Classification:

Class II

Date Initiated: March 3, 2016

Date Posted: July 6, 2016

Recall Number: Z-2057-2016

Event ID: 73584

Reason for Recall:

Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen containers were packed in incorrect exterior carton.

Status: Terminated

Product Quantity: 399 cases/25 sleeves/20 cups & lids per sleeve

Code Information:

Lot Numbers: 31899, 32014, 32015, 32410 & 32411

Distribution Pattern:

US Nationwide in the states of AL, AR, FL, GA, MA, NC, NY, NJ, NH, PA, OH, TX & VA; International: Canada

Voluntary or Mandated:

Voluntary: Firm initiated