Fresh Recalls

FDAClass II · Medical device · Recall Z-2309-2026 · Recalled June 10, 2026

Sharpoint 2 recall — SSC- Surgical Specialties Corporation

Agency report date: June 10, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Sharpoint 2
Company / brand
SSC- Surgical Specialties
Lot / serial / date codes
UDI-DI 00848782027514; Lot Number FA22CHQ
Distribution
Worldwide - US Nationwide distribution in the states of Texas, Utah, Michigan and the countries of Turkey, Germany, Romania, Poland, United Kingdom.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Sharpoint 2 recall status

3. Open the official notice or contact

Official recall ID
Z-2309-2026
Brand
All SSC- Surgical Specialties recalls
Classification
Class II
Units affected
1818 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Chula Vista, CA, United States
Firm address
1690 Brandywine Ave Ste C, 91911-6072

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI 00848782027514; Lot Number FA22CHQ
Distribution
Worldwide - US Nationwide distribution in the states of Texas, Utah, Michigan and the countries of Turkey, Germany, Romania, Poland, United Kingdom.
Firm notified the public via
E-Mail
FDA event ID
98911
Recall initiated
April 23, 2026
FDA classified
June 4, 2026
FDA report date
June 10, 2026

Other medical device recalls from around the same time

Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 8, 2026 at 6:00 PM UTC.

Report a data error on this page