Reported Jul 11, 2018 · Terminated

Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery

Beaver Visitec

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Beaver Visitec · 500 Totten Pond Rd · Waltham, MA · 02451-1916

Is this the product you have?

  • Safety Sideport Knife 1.0mm 45¿
  • REF 378210 Product UsageIndicated to make stab incisions during ophthalmic surgery
Lot codes and dates
  • Lot Numbers6002436 & 6002663
Amount recalled
1354 units

Where it was sold

Why it was recalled

Blades are loose in handles and may fall out due to non cured epoxy

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 8, 2021 · Data as of Sep 19, 6:53 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.