Recall Z-1163-2021— Johnson & Johnson Surgical Vision Inc
Class II · Terminated
Class II FDA medical device recall by Johnson & Johnson Surgical Vision Inc, initiated 2021-01-27, terminated 2022-11-09. FDA's recall record names no specific 510(k) clearance for this event. Product: TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.. Reason: Due to the release of nonconforming Intraocular Lenses (IOLs)..
- Recalling firm
- Johnson & Johnson Surgical Vision Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-01-27
- Terminated
- 2022-11-09
- Firm location
- Santa Ana, CA, United States
Product description
TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.
Reason for recall
Due to the release of nonconforming Intraocular Lenses (IOLs).
Data sourced from openFDA. This site is unofficial and independent of the FDA.