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Sharpoint recallZ-2309-2026 · SSC- Surgical Specialties Corporation · initiated Apr 23, 2026

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from SSC- Surgical Specialties Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.

FDA root cause category: Mixed-up of materials/components

What the company is doing

On August 22, 2026, Surgical Specialties Corp. (subsidiary of Corza Medical) issued a Urgent Medical Device recall notification via E.Mail to affected consignees. Surgical Specialties ask consignees to take the following actions: 1. Immediately examine your inventory and quarantine product subject to recall. We request the return of any affected product that may still be in your inventory. We will replace the product 2. Recall Acknowledgement & Receipt Please complete and return the attached Medical Device Recall Acknowledgement & Receipt form as soon as possible to [email protected]. 3. To initiate a return, contact [email protected] to process the request. 4. If you have any questions related to product quality, contact us at [email protected].

Recall details

Recall number
Z-2309-2026
Status
Open, Classified
Initiated by the company
Apr 23, 2026
Posted by the FDA
Jun 4, 2026
Recalling firm
SSC- Surgical Specialties Corporation
Quantity
1818 units
Product code
HNN
Distribution
Worldwide - US Nationwide distribution in the states of Texas, Utah, Michigan and the countries of Turkey, Germany, Romania, Poland, United Kingdom.

Product description

Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife

Code information (models, lots, serial numbers)

UDI-DI 00848782027514; Lot Number FA22CHQ

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Product lines

Sources and updates

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