Fresh Recalls

FDAClass II · Medical device · Recall Z-2934-2026 · Recalled August 19, 2026

Endo-Model recall — Waldemar Link GmbH & Co. KG (Mfg Site)

Agency report date: August 19, 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
Endo-Model
Company / brand
Waldemar Link & Co. KG (Mfg Site)
Lot / serial / date codes
UDI-DI 04026575432134 Lot for Implant REF 15-0027/16: 2604069
Distribution
Domestic US distribution to Indiana. OUS distribution to Belarus and Germany.
Agency product description and boundaries

Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16

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: The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted and an alternative product would be needed. If the incorrect plateau were to be implanted, this is associated with increased risk of wear, which could result in a reduced standing time of the implant.

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: Endo-Model

3. Open the official notice or contact

Official recall ID
Z-2934-2026
Brand
Waldemar Link & Co. KG (Mfg Site)
Classification
Class II
Units affected
1 US; 9 OUS
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Norderstedt, Germany
Firm address
Ost Str. 4-10, N/A

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI 04026575432134 Lot for Implant REF 15-0027/16: 2604069
Distribution
Domestic US distribution to Indiana. OUS distribution to Belarus and Germany.
Firm notified the public via
Letter
FDA event ID
99405
Recall initiated
July 6, 2026
FDA classified
August 11, 2026
FDA report date
August 19, 2026
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 September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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