SSC- Surgical Specialties Corporation recalls Sharpoint 2.2MM
Reason for recall
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
Lot / code information
- UDI
- 00848782027514
- Lot #
- FA22CHQ
What the firm 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 returns.corzaeye@corza.com. 3. To initiate a return, contact returns.corzaeye@corza.com to process the request. 4. If you have any questions related to product quality, contact us at complaints@corza.com.
DistributionShow detailsHide
Worldwide - US Nationwide distribution in the states of Texas, Utah, Michigan and the countries of Turkey, Germany, Romania, Poland, United Kingdom.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2309-2026
- FDA device classification · HNNOfficial FDA classification for this device type
- CFR regulation · 21 CFR 886.4350The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find SSC- Surgical Specialties CorporationSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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