Treatment packs used on the VisuMax Laser Keratome recall
Treatment packs used on the VisuMax Laser Keratome. Size M Manufactured by Carl Zeiss Meditec AG, Jena, Germany. The VisuMax Laser Keratome is…
Why was Treatment packs used on the VisuMax Laser Keratome recalled?
Carl Zeiss Treatment pack, lot number M 130010, size M, may actually contain size S.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
P/N 1462-333, Size M, Lot # M130010
- Product
- Treatment packs used on the VisuMax Laser Keratome. Size M Manufactured by Carl Zeiss Meditec AG, Jena, Germany. The VisuMax Laser Keratome is…
- Recalling firm
- Carl Zeiss Meditec AG
- Quantity
- 1 package containing 10 individual treatment packs
- Distribution
- US Distribution: NV only.
- Recall date
- March 19, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)