Endoscopic Kittner Blunt Dissecting Instrument recall: Sterility Concern
Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
Why was Endoscopic Kittner Blunt Dissecting Instrument recalled?
The affected products may have been packaged with a defect in the sterile barrier seal. As a result, the integrity of the sterile barrier may be compromised.
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?
UDI-DI: 00840113214006; Lot Numbers: 389571, 389576, 390981, 390982
- Product
- Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
- Recalling firm
- ASPEN SURGICAL
- Quantity
- 1900 units
- Distribution
- US Nationwide
- Recall date
- July 3, 2024
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)