FDAClass IINovember 16, 2022

Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an recall

Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an orthopedic blade, which may be used in various types of orthopedic surgery (i.e. foot, ankle, hand…

Why was Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an recalled?

Incorrect configuration of the blades in the package. The blades curve to the right instead of curving to the left. If used may cause cause unintended tissue damage during the procedure or if noticed prior to use may cause a delay in surgery

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

UDI# 00886158001249 LOT#'s: 6034831,6039837

Product
Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an orthopedic blade, which may be used in various types of orthopedic surgery (i.e. foot, ankle, hand…
Recalling firm
Beaver Visitec International, Inc.
Quantity
150 units US; 1116 units OUS
Distribution
FL, GA, IN, LA, MA, ME, VA Foreign: France, Japan, Netherlands, Switzerland, United Kingdom
Recall date
November 16, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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