CLASS II ONGOING Device recall · Reported 10 Jun 2026 · FDA Enforcement Report
Sharpoint, Angled, Double- Bevel recalled by SSC- Surgical Specialties
SSC- Surgical Specialties is recalling Sharpoint, Angled, Double- Bevel, distributed nationwide in the US. The recall was initiated on 23 Apr 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2309-2026
- FDA event ID
- 98911
- Recalling firm
- SSC- Surgical Specialties, Chula Vista, CA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 23 Apr 2026
- FDA classified
- 4 Jun 2026
- Reported
- 10 Jun 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Packaging Defects
- Device type
- Surgical Instruments
Timeline
| 23 Apr 2026 | Recall initiated by company | |
| 4 Jun 2026 | Classified by FDA | +42 days |
| 10 Jun 2026 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
Where it was distributed
Worldwide - US Nationwide distribution in the states of Texas, Utah, Michigan and the countries of Turkey, Germany, Romania, Poland, United Kingdom.
Questions about this recall
Why was it recalled?
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
Which lots are affected?
UDI-DI 00848782027514; Lot Number FA22CHQ
Where was it sold?
Worldwide - US Nationwide distribution in the states of Texas, Utah, Michigan and the countries of Turkey, Germany, Romania, Poland, United Kingdom.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from SSC- Surgical Specialties
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Sharpoint Polypropylene Blue Monofilament 6" recalled | SSC- Surgical Specialties | Other | 9 states |
Other Surgical Instruments recalls
All 3,891| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Adaptable Beach Chair Beach Chair surgical patient positioner recalled | Quantum OPS | Device Malfunction | Nationwide |
| Device | CLASS II | Laparoscopic Prostatectomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Halyard Laparoscopy Comprehensive Pack II recalled | GRI Medical & Electronic Technology | Other | Nationwide |
| Device | CLASS II | Gyn Laparoscopy/Laparotomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Gyn Laparoscopy Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |