fda
3 records
FDA Device Recall: PROKERA Plus, non-sterile - Product Usage: Biologic corneal bandage.
2020-12-16
Class II — Potential exposure of product to microbial contamination.
View Source
FDA Device Recall: PROKERA, non-sterile - Product Usage: Biologic corneal bandage.
2020-12-16
Class II — Potential exposure of product to microbial contamination.
View Source
FDA Device Recall: PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage.
2020-12-16
Class II — Potential exposure of product to microbial contamination.
View Source
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