Z-0552-2021 Class II Terminated
FDA device recall Z-0552-2021 was initiated by TissueTech, Inc. on November 10, 2020 and is designated Class II. Reason for recall: Potential exposure of product to microbial contamination. The recall status is terminated (terminated July 6, 2023). Affected quantity: 75 units.
Recall Details
- Product Type
- Devices
- Report Date
- December 16, 2020
- Initiation Date
- November 10, 2020
- Termination Date
- July 6, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 75 units
Product Description
PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage.
Reason for Recall
Potential exposure of product to microbial contamination.
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.
Code Information
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