Medical device recalls

Beaver Visitec recalls Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for ophtha…

Recall date
February 19, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1088-2019
FDA classification
Class III
Brand / firm
Beaver Visitec
Sold / distributed
US Nationwide Distribution to states of : AL, AZ, CA, FL, ID, MN, MO, NY, OH, PA, and TX; and internationally to: Ireland and UK.

Why it was recalled

The product contains a misprinted expiration date on the peel pack. Both were printed as "180615", which is the lot number. The Lot number is correct.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. .

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