Recall Z-2342-2018— Beaver Visitec
Class II · Terminated
Class II FDA medical device recall by Beaver Visitec, initiated 2018-05-14, terminated 2021-06-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery. Reason: Blades are loose in handles and may fall out due to non cured epoxy.
- Recalling firm
- Beaver Visitec
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-05-14
- Terminated
- 2021-06-08
- Firm location
- Waltham, MA, United States
Product description
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Reason for recall
Blades are loose in handles and may fall out due to non cured epoxy
Data sourced from openFDA. This site is unofficial and independent of the FDA.