Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains a misprinted expiration date on...

Date: February 19, 2019
Company: Beaver Visitec
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Beaver Visitec directly.

Affected Products

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. .

Quantity: 97 boxes (10units/box)

Why Was This 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.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Beaver Visitec

Beaver Visitec has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report