Safety Sideport Knife 1.0mm 45¿ recall
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Why was Safety Sideport Knife 1.0mm 45¿ recalled?
Blades are loose in handles and may fall out due to non cured epoxy
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?
Lot Numbers: 6002436 & 6002663
- Product
- Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
- Recalling firm
- Beaver Visitec
- Quantity
- 1354 units
- Distribution
- US Nationwide in the states of CA, IA, CO, HI, IA, MD & TX
- Recall date
- July 11, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)