Fresh Recalls

FDAClass II · Medical device · Recall Z-3018-2026 · Recalled September 2, 2026

CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5 recall — ConMed Corporation

Agency report date: September 2, 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
CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5
Company / brand
ConMed
Lot / serial / date codes
UDI:10845854042472, Lot number 1513167
Distribution
US Nationwide distribution in the state of TX.
Agency product description and boundaries

CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures Sterile

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: Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.

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: CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5 recall status

3. Open the official notice or contact

Official recall ID
Z-3018-2026
Brand
All ConMed recalls
Classification
Class II
Units affected
2 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Utica, NY, United States
Firm address
525 French Rd, N/A, 13502-5945

Identifying details (verbatim from the notice)

Product codes / lots
UDI:10845854042472, Lot number 1513167
Distribution
US Nationwide distribution in the state of TX.
Firm notified the public via
E-Mail
FDA event ID
99498
Recall initiated
July 14, 2026
FDA classified
August 26, 2026
FDA report date
September 2, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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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 October 22, 2026 at 6:00 PM UTC.

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