TissueTech, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0551-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

PROKERA Plus, non-sterile - Product Usage: Biologic corneal bandage.

Product Classification:

Class II

Date Initiated: November 10, 2020

Date Posted: December 16, 2020

Recall Number: Z-0551-2021

Event ID: 86807

Reason for Recall:

Potential exposure of product to microbial contamination.

Status: Terminated

Product Quantity: 10 units

Code Information:

Lot Codes: BTR192864, BTR194678, BTR192872, BTR193024 Serial ID: 20-PKP-00994,20-PKP-00988,20-PKP-00989,20-PKP-00990,20-PKP-00991,20-PKP-00992,20-PKP-00993,20-PKP-00995,20-PKP-00996, and 20-PKP-00997

Distribution Pattern:

US Nationwide distribution including in the states of FL, MN, NY, NC, SC, NJ, GA, PA, MD, DC, OH, WA, MI, CO, KS, TN, ME, AL, AR, TX, KY, MA, CA, CT, and OK.

Voluntary or Mandated:

Voluntary: Firm initiated