Microline Surgical, Inc.: Microscissor Tip (Disposable); Microline Catalog #: 3122.

Recall number

Z-0663-2025

Recalling firm

Microline Surgical, Inc.

Product

Microscissor Tip (Disposable); Microline Catalog #: 3122.

Status

Open, Classified

Initiated

2024-11-05

Posted

2024-12-10

Terminated

not on file

Reason

A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of the heat shrink breaking off.

Root cause

Under Investigation by firm

Action

On November 6, 2024 URGENT: MEDICAL DEVICE RECALL letters were sent to consignees. Actions to be taken by the Customer/User: Please locate those products you have that correspond with the above identified lots, quarantine them, and arrange for their return by contacting Microline Customer Service to receive an RMA number. Alternatively, you may wish to contact your Microline Distributor or Sales Representative to help with this. If you have used some or all of the identified product, please provide the item number, lot number, and the amount used so that we can track the progress of the recall. All products returned will be replaced at no cost. This recall is being done in an abundance of caution. No other item numbers or lots of ReNew Disposable Tips are affected by this recall. If you experience any adverse events or quality problems with the use of this product, please be sure to report this to the relevant Competent Authority s Adverse Event Reporting Program and to Microline as soon as possible. We regret any inconvenience and encourage you to contact Microline Customer Service at 978- 922-9810 or info@microlinesurgical.com. with any further questions. Actions to be taken by the Distributor: 1. Immediately determine if you are in possession of the products subject to this recall by checking the product name, item number, and lot number. 2. If you are a distributor of products subject to this recall, we require that you immediately remove affected products from inventory, quarantine products, and stop sales and shipping. 3. If you are a distributor and you have further distributed products subject to this recall, please identify customers immediately and notify them of this product recall using this Recall Notification Letter. Translation of this letter into local language is acceptable. We request that you direct your customers to return affected products to your facility for subsequent return to Microline. The relevant Competent Authority will be monitoring th

Quantity

200 units

Distribution

Worldwide - US Nationwide in the state of OK and the country of Japan.

Lot, serial or model codes

Microline Catalog #: 3122; UDI/DI: 811099010036; Lot Number: 00172110.

510(k) numbers

["K213127"]

PMA numbers

not on file

Product code

GEI

Firm FEI

1000137656

Firm city

Beverly

Firm state

MA

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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