FDA Enforcement Class II Terminated

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

Recall: Z-0552-2021 · Reported December 16, 2020

Enforcement

Recall Number
Z-0552-2021
Event ID
86807
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
TissueTech, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
December 16, 2020
Initiation Date
November 10, 2020
Classification Date
December 9, 2020
Termination Date
July 6, 2023
Address
8305 NW 27th St Ste 101, N/A, Doral, FL, 33122-1934, United States

Description

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

Reason

Potential exposure of product to microbial contamination.

Code Info

Lot Codes: BTR192864, BTR194678, BTR192872, BTR193024 Serial ID: 20-PKS-14212,20-PKS-14213,20-PKS-14214,20-PKS-14215,20-PKS-14216,20-PKS-14217,20-PKS-14218,20-PKS-14219,20-PKS-14202,20-PKS-14203,20-PKS-14204,20-PKS-14205,20-PKS-14191,20-PKS-14192,20-PKS-14193,20-PKS-14194,20-PKS-14195,20-PKS-14196,20-PKS-14197,20-PKS-14198,20-PKS-14199,20-PKS-14200,20-PKS-14207,20-PKS-14208,20-PKS-14209,20-PKS-14210,20-PKS-14211,20-PKS-14206,20-PKS-14188,20-PKS-14189,20-PKS-14190,20-PKS-14201,20-PKS-14304,20-PKS-14272,20-PKS-14273,20-PKS-14274,20-PKS-14275,20-PKS-14276,20-PKS-14277,20-PKS-14290,20-PKS-14291,20-PKS-14292,20-PKS-14293,20-PKS-14294,20-PKS-14278,20-PKS-14279,20-PKS-14280,20-PKS-14297,20-PKS-14307,20-PKS-14308,20-PKS-14298,20-PKS-14309,20-PKS-14310,20-PKS-14311,20-PKS-14312,20-PKS-14313,20-PKS-14281,20-PKS-14282,20-PKS-14283,20-PKS-14284,20-PKS-14285,20-PKS-14286,20-PKS-14287,20-PKS-14288,20-PKS-14289,20-PKS-14305,20-PKS-14306,20-PKS-14295,20-PKS-14296,20-PKS-14314,20-PKS-14299,20-PKS-14300,20-PKS-14301,20-PKS-14302, and 20-PKS-14303

Distribution

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.

Quantity

75 units