EIT CIF cage recall
EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients…
Why was EIT CIF cage recalled?
Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI-DI: 04260557770658 Lot Number: E20CL0603
- Product
- EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients…
- Recalling firm
- DePuy Spine, Inc.
- Quantity
- 61 units
- Distribution
- Distribution US Nationwide
- Recall date
- July 13, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)