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No linked recall records

Allure Hip Stem

WALDEMAR LINK GmbH & Co. KG · Hip implants

FDA device identifier records list Allure Hip Stem under WALDEMAR LINK GmbH & Co. KG. This page lists 52 device model identifiers in Hip implants; source families may also contain components and instruments. UDI listing identifies products; it does not establish FDA approval or recall status.

No recall records are linked to this device in MedWatcher’s published dataset. Coverage is limited, and newer records may not yet be included.

Published Aug 18, 2026Device details updated Oct 26, 2026Latest linked source check: 2026-10-27 00:14:26 UTC

Source checks below cover individual records. A manufacturer product-page check confirms device identity; it does not confirm recall status.

Recall records referencing this device

No recall records are currently linked here. This is not a complete recall search or a statement that the product is safe or appropriate for you. Search the FDA recall database using the device name and manufacturer, then compare the model and serial or lot numbers with your device.

FDA-associated products and identifiers

These identity records can cover devices, accessories or software associated with this name. They do not establish FDA approval or identify which products are affected by a recall. Compare your label with the official record; recall scope is listed separately below.

Find a model, catalogue number or primary DI

Showing 1–20 of 52 identity records

FDA-associated product and identifier records, separate from recall scope
Model / version	Catalogue number	Primary device identifier
296-001/01	Not listed	04026575447831 — FDA record (opens in a new tab)
296-001/02	Not listed	04026575447848 — FDA record (opens in a new tab)
296-001/03	Not listed	04026575447855 — FDA record (opens in a new tab)
296-001/04	Not listed	04026575447862 — FDA record (opens in a new tab)
296-001/05	Not listed	04026575447879 — FDA record (opens in a new tab)
296-001/06	Not listed	04026575447886 — FDA record (opens in a new tab)
296-001/07	Not listed	04026575447893 — FDA record (opens in a new tab)
296-001/08	Not listed	04026575447909 — FDA record (opens in a new tab)
296-001/09	Not listed	04026575447916 — FDA record (opens in a new tab)
296-001/10	Not listed	04026575447923 — FDA record (opens in a new tab)
296-001/11	Not listed	04026575447930 — FDA record (opens in a new tab)
296-001/12	Not listed	04026575447947 — FDA record (opens in a new tab)
296-001/13	Not listed	04026575447954 — FDA record (opens in a new tab)
296-002/01	Not listed	04026575447961 — FDA record (opens in a new tab)
296-002/02	Not listed	04026575447978 — FDA record (opens in a new tab)
296-002/03	Not listed	04026575447985 — FDA record (opens in a new tab)
296-002/04	Not listed	04026575447992 — FDA record (opens in a new tab)
296-002/05	Not listed	04026575448005 — FDA record (opens in a new tab)
296-002/06	Not listed	04026575448012 — FDA record (opens in a new tab)
296-002/07	Not listed	04026575448029 — FDA record (opens in a new tab)

Device facts

Manufacturer: WALDEMAR LINK GmbH & Co. KG
Category: Hip implants
FDA generic device type: Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Official sources

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-004/07

Identifier: Primary DI 04026575447763
Published: Nov 21, 2025
Source checked: 2026-10-27 00:14:26 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-002/08

Identifier: Primary DI 04026575448036
Published: Nov 21, 2025
Source checked: 2026-10-27 00:13:56 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-004/08

Identifier: Primary DI 04026575447770
Published: Nov 21, 2025
Source checked: 2026-10-27 00:08:22 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-003/09

Identifier: Primary DI 04026575447657
Published: Nov 21, 2025
Source checked: 2026-10-27 00:08:14 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-003/07

Identifier: Primary DI 04026575447633
Published: Nov 21, 2025
Source checked: 2026-10-27 00:07:43 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

Showing 5 of 52 linked source records. Use the identifier list for additional product records. Recall pages link to their official sources.

How MedWatcher checks these sources

Actinia®

implantcast GmbH · Hip implants

No linked recall records

Latest source check Oct 27, 2026

Alloclassic®

Zimmer GmbH · Hip implants

No linked recall records

Latest source check Oct 27, 2026

Alpine

Ortho Development Corporation · Hip implants

No linked recall records

Latest source check Oct 27, 2026

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Image unavailable

No linked recall records

Allure Hip Stem

WALDEMAR LINK GmbH & Co. KG · Hip implants

No recall records are linked to this device in MedWatcher’s published dataset. Coverage is limited, and newer records may not yet be included.

Published Aug 18, 2026Device details updated Oct 26, 2026Latest linked source check: 2026-10-27 00:14:26 UTC

Source checks below cover individual records. A manufacturer product-page check confirms device identity; it does not confirm recall status.

Recall records referencing this device

FDA-associated products and identifiers

Find a model, catalogue number or primary DI

Showing 1–20 of 52 identity records

FDA-associated product and identifier records, separate from recall scope
Model / version	Catalogue number	Primary device identifier
296-001/01	Not listed	04026575447831 — FDA record (opens in a new tab)
296-001/02	Not listed	04026575447848 — FDA record (opens in a new tab)
296-001/03	Not listed	04026575447855 — FDA record (opens in a new tab)
296-001/04	Not listed	04026575447862 — FDA record (opens in a new tab)
296-001/05	Not listed	04026575447879 — FDA record (opens in a new tab)
296-001/06	Not listed	04026575447886 — FDA record (opens in a new tab)
296-001/07	Not listed	04026575447893 — FDA record (opens in a new tab)
296-001/08	Not listed	04026575447909 — FDA record (opens in a new tab)
296-001/09	Not listed	04026575447916 — FDA record (opens in a new tab)
296-001/10	Not listed	04026575447923 — FDA record (opens in a new tab)
296-001/11	Not listed	04026575447930 — FDA record (opens in a new tab)
296-001/12	Not listed	04026575447947 — FDA record (opens in a new tab)
296-001/13	Not listed	04026575447954 — FDA record (opens in a new tab)
296-002/01	Not listed	04026575447961 — FDA record (opens in a new tab)
296-002/02	Not listed	04026575447978 — FDA record (opens in a new tab)
296-002/03	Not listed	04026575447985 — FDA record (opens in a new tab)
296-002/04	Not listed	04026575447992 — FDA record (opens in a new tab)
296-002/05	Not listed	04026575448005 — FDA record (opens in a new tab)
296-002/06	Not listed	04026575448012 — FDA record (opens in a new tab)
296-002/07	Not listed	04026575448029 — FDA record (opens in a new tab)

Device facts

Manufacturer: WALDEMAR LINK GmbH & Co. KG
Category: Hip implants
FDA generic device type: Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Official sources

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-004/07

Identifier: Primary DI 04026575447763
Published: Nov 21, 2025
Source checked: 2026-10-27 00:14:26 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-002/08

Identifier: Primary DI 04026575448036
Published: Nov 21, 2025
Source checked: 2026-10-27 00:13:56 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-004/08

Identifier: Primary DI 04026575447770
Published: Nov 21, 2025
Source checked: 2026-10-27 00:08:22 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-003/09

Identifier: Primary DI 04026575447657
Published: Nov 21, 2025
Source checked: 2026-10-27 00:08:14 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

FDA Global Unique Device Identification Database

Allure Hip Stem — Device model — 296-003/07

Identifier: Primary DI 04026575447633
Published: Nov 21, 2025
Source checked: 2026-10-27 00:07:43 UTC

Exact primary identifier, current FDA source, company identity, explicit family grouping, category consistency and duplicate checks passed. This is automated validation, not human or clinical review.

View official record

Showing 5 of 52 linked source records. Use the identifier list for additional product records. Recall pages link to their official sources.

How MedWatcher checks these sources

Actinia®

implantcast GmbH · Hip implants

No linked recall records

Latest source check Oct 27, 2026

Alloclassic®

Zimmer GmbH · Hip implants

No linked recall records

Latest source check Oct 27, 2026

Alpine

Ortho Development Corporation · Hip implants

No linked recall records

Latest source check Oct 27, 2026

Allure Hip Stem

Follow Allure Hip Stem

Recall records referencing this device

FDA-associated products and identifiers

Device facts

Allure Hip Stem

Follow Allure Hip Stem

Recall records referencing this device

FDA-associated products and identifiers

Device facts