Microscissor Tip (Disposable); Microline Catalog #: 3122.
FDA Recall Z-0663-2025 · Posted 2024-12-10
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Recalling FirmMicroline Surgical, Inc.
Recall StatusOpen, Classified
Product CodeGEI
Date Initiated2024-11-05
Product Quantity200 units
Reason for Recall
A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of the heat shrink breaking off.
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 [email protected]. 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
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide - US Nationwide in the state of OK and the country of Japan.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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